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Chronic photoperiodic manipulation induced chronodisruption upregulates HSP60 during early pro-atherogenic remodeling in thoracic aorta of C57BL/6J mice

Abstract

Background

Circadian disruption is often associated with aggravation of atherosclerosis; however, the pathophysiological mechanisms underlying atherogenic initiation in normolipidemic diet remains unclear. Most of the studies done for understanding circadian disruption induced atherosclerosis have been carried out in murine model of hyperlipidemia induced atherosclerosis. The present study investigates pro-atherogenic events in response to chronic photoperiodic manipulation induced chronodisruption (PMCD) in C57BL/6J mice fed with laboratory chow diet.

Results

The results were compared with atherogenic initiation induced by high fat high fructose (HFHF) diet. The combined effects of HFHF and PMCD on atherogenic initiation were also investigated for possible synergy of both variants. The HFHF and HFHF+PMCD groups recorded increments in body weight gains and serum lipid parameters (TC, TG, LDL-cholesterol, VLDL) and a decrement in HDL-cholesterol as compared to the control group. However, PMCD group recorded body weight gain similar to that of the control group, but the serum lipid parameters (TG and VLDL) were significantly elevated and the HDL levels were lowered. However, prominent hypertrophic remodeling, higher collagen deposition, and elastin derangement, along with endothelial dysfunction, its activation, and macrophage infiltration, were observed in thoracic aorta of all the three experimental groups. But the mRNA and immunoblots of heat shock protein 60 (HSP60) in thoracic aorta was found to be maximum in PMCD followed by HFHF and HFHF+PMCD groups.

Conclusion

Laboratory chow feeding coupled with photoperiodic manipulation mediated chronodisruption overexpress HSP60 that in turn plays a central role in PMCD mediated pro-atherogenic remodeling in thoracic aorta of C57BL/6J mice.

Background

Intrinsic circadian clock is known to regulate synchrony of physiological processes in the body. Disturbance in biological rhythm due to the long working hours, shift jobs, and transcontinental travel is strongly associated with metabolic disorders. Epidemiological studies had demonstrated that shift workers comprise of a higher risk group for cardiovascular manifestations (Hermansson et al., 2019; Scheer, Hilton, Mantzoros, & Shea, 2009). A cross-sectional study with night shift workers had suggested association of shift work with increased arterial stiffness that mark early atherogenic change (Jankowiak et al., 2016). Another observational study with factory workers had associated photoperiodic shifts with cardiovascular mortality (Knutsson, Hammar, & Karlsson, 2004). Clinical studies had shown that acute cardiovascular events follow diurnal pattern indicating involvement of circadian clock components (Muller et al., 1985; Willich, 1990). In this regard, deletion or mutation of various circadian genes in murine models of atherosclerosis had been observed to promote plaque formation (Anea et al., 2009; Somanath et al., 2011). Western diet-induced lesion formation in aortic root was reported to be aggravated in ApoE*3-Leiden.CETP mice subjected to alternating light-dark conditions (Schilperoort et al., 2020). Thus, circadian disruption or photoperiodic alterations is an addition to the risk factors for atherosclerosis. Because of its multifactorial nature, the pathogenic mechanism underlying the atherogenic initiation need absolute clarity but till date, many facets remain unexplored.

Atherosclerosis is primarily associated with hyperlipidemia; however, majority of patients have been reported to have cholesterol levels within the normal range, suggesting a pathogenic mechanism independent of lipid levels (Fernandez-Friera et al., 2017; Ridker et al., 2008; Sniderman et al., 1980). Under such circumstances, the auto-antigenic role of heat shock protein 60 (HSP60) has emerged as a plausible explanation for the atherogenic initiation (Grundtman & Wick, 2011). Serum levels of soluble HSP60 and autoreactive antibodies have been strongly correlated with atherosclerotic plaque severity (Xu et al., 1993; Xu et al., 1999; Xu et al., 2000). Also, ectopic expression of HSP60 in endothelial cells exposed to classical atherogenic risk factors has been observed (Amberger et al., 1997; Hochleitner et al., 2000; Jakic, Buszko, Cappellano, & Wick, 2017; Kreutmayer et al., 2011). Simultaneous expression of adhesion molecules in stressed endothelium facilitates the sub-endothelial infiltration of leukocytes, thus promoting inflammation. In this context, accumulation of HSP60-autoreactive T cells has been reported to be the first event during atherogenic initiation in human aorta (Almanzar et al., 2012). Similarly, intravenous injection of bacterial lipopolysaccharides (LPS) in normocholesterolemic rabbits had upregulated intracellular adhesion molecule-1 (ICAM-1) and HSP60 expression in the arteries fulfilling the prerequisite for autoreactive T cell recruitment (Seitz, Kleindienst, Xu, & Wick, 1996). These changes are often accompanied by vascular dysfunction causing detrimental effects on the vascular tone leading to arterial stiffness. The infiltration of mononuclear cells in the vascular wall also causes inflammation contributing to the overall progression of the disease.

Atherogenic risk factors such as bacterial LPS, inflammatory cytokines, cigarette smoke extract, fluid shear stress, chlamydial infection, and hypertension have been associated with HSP60 induction in vascular endothelium (Amberger et al., 1997; Hochleitner et al., 2000; Jakic et al., 2017; Kreutmayer et al., 2011; Kreutmayer et al., 2013). Two cross-sectional studies with clinically healthy young males and females showed increased intima-media thickening that correlated with T cell reactivity against HSP60 wherein active and passive smoking were found to be major associated risk factors, respectively (Knoflach et al., 2003; Knoflach et al., 2009). High fat diet and atherogenic diet induced HSP60 expression have also been reported in atherosclerotic plaques of ApoE−/− mice (Zhao et al., 2015). Thus, the upregulation of HSP60 in vascular wall has been acknowledged as a central mediator of atherogenic initiation, but the same has not been explored in the context of photoperiodic stress-induced atherosclerosis.

In light of these reports, the present study assesses atherogenic remodeling of thoracic aorta of C57BL/6J mice subjected to photoperiodic manipulation induced chronodisruption. High fat high fructose diet (HFHF) fed mice have been used as the disease positive control. A combination of HFHF+PMCD has also been put to scientific scrutiny to assess the possible synergistic effect on atherogenic transformation. Cause/s for pro-atherogenic changes in a normolipidemic condition is also investigated herein.

Materials and methods

Animal experiments

C57BL/6J male mice (20–22 g) of age 4–6 weeks were obtained from Advanced Center for Treatment, Research and Education in Cancer (ACTREC), Navi Mumbai, India. Mice were housed as 3–5 per cage and maintained as per the guidelines of the Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA) at the animal house of Department of Zoology, The Maharaja Sayajirao University of Baroda, Vadodara, Gujarat, India (827/GO/Re/S/04/CPCSEA). The animal experiment protocol (MSU-Z/IAEC/2/09-2017) was approved by the Institutional Animal Ethical Committee (IAEC), Department of Zoology, The Maharaja Sayajirao University of Baroda, and the experiments were conducted in accordance with the guidelines of CPCSEA. Mice were fed ad libitum with standard laboratory chow and water in rooms maintained in 12 h light/12 h dark cycle at 23 to 25 °C with humidity between 50–70%. After 10 days of acclimatization, mice were randomly divided into four groups: control group (n = 6, fed with standard chow and subjected to normal 12:12 light/dark cycle), high fat high fructose (HFHF) group (n = 10, fed with high fat diet containing 35.3% fat content and 20% fructose in water and subjected to normal 12:12 light-dark cycle), the photoperiodic manipulation induced chronodisruption (PCMD) group (n = 10, fed with standard chow and subjected to photoperiodic manipulation induced chronodisruption), and the HFHF+PMCD group (n = 10, fed with HFHF and subjected to PMCD). Mice undergoing photoperiodic manipulation induced chronodisruption were transferred from room 1 (7:00 to 19:00 h light/19:00 to 7:00 h dark period) to room 2 (11:00 to 23:00 h dark/23:00 to 11:00 h light period) resulting in phase advance of 8 h (lights off at ZT4) and transferring back to room 1 resulting in a phase delay of 8 h (lights off at ZT20) (Fig. 1) on Mondays and Thursdays, respectively, at 10:55 h (Kettner et al., 2015). Food intake and body weight were recorded every alternate day. At the end of 16 weeks, blood was collected from mice via retro-orbital sinus after overnight fasting and later were euthanized with mild isoflurane. The thoracic aortas were excised, fixed in 4% buffered paraformaldehyde (PFA), and embedded in paraffin using standard protocol for histochemical analysis. For gene expression studies, the tissue samples were snap frozen in liquid nitrogen and stored at − 80 °C until use. Serum was isolated from blood using standard protocol and was subjected to analysis of triglycerides (TG), total cholesterol (TC), very low density lipoprotein (VLDL), low density lipoprotein-cholesterol (LDL-Chol), and high density lipoprotein-cholesterol (HDL-Chol) using commercially available kits (Reckon Diagnostic kits, Vadodara, Gujarat, India).

Fig. 1
figure1

Schematic representation of photoperiodic regime. C57BL/6J mice of control and HFHF groups L:D 12:12; PMCD were subjected to 8 h phase advance on Monday and 8 h phase delay on Thursday for 16 weeks resulting in chronodisruption, whereas HFHF+PMCD were fed with high fat high fructose (HFHF) diet and maintained on PMCD photoperiodic regimen

Histology and morphometric analysis

PFA fixed thoracic aorta were dehydrated in a graded series of ethanol and embedded in paraffin blocks. Five to 6 μm serial sections were cut using microtome and stained with hematoxylin-eosin (HXE; Sigma-Aldrich, USA). The sections were observed using Leica DMRB microscope (Leica Camera Inc., Germany) and images were captured. The intima-media thickness (IMT) and lumen area were measured using ImageJ software (NIH, Bethesda, USA) by an investigator blinded to experimental groups.

Elastin auto-fluorescence

Elastin auto-fluorescence was recorded from the HXE stained sections (Sawada & Daugherty, 2018) using Floid imaging station (Life Technologies, USA). Elastin breaks, defined as discontinuity of an elastic fiber with boundaries at both sides clearly visible, were counted from the sections.

Collagen staining

Paraffin-embedded sections were de-paraffinized with xylene and rehydrated in a graded series of ethanol followed by staining with 0.1% direct red 80 (Sigma-Aldrich, USA) in saturated aqueous solution of picric acid for 1 h at room temperature (RT). Sections were observed under Leica DMRB microscope (Leica Camera Inc., Germany) and images were captured. Quantitative analysis of the images for collagen and elastin content was done using ImageJ software (NIH, Bethesda, USA) (Borges, Taboga, & Gutierrez, 2005; Vogel, Siebert, Hofmann, & Frantz, 2015) and aortic stiffness was calculated as ratio of collagen to elastin.

Immunohistochemical analysis

Paraffin-embedded sections of thoracic aorta were subjected to immunohistochemical staining for detection of HSP60 or CD68. Briefly, 5–6 μm sections were cut and de-paraffinized in xylene followed by re-hydration using graded series of ethanol. Sections were subjected to antigen retrieval in sodium citrate buffer at 95 °C for 20 min and endogenous peroxidases were masked with 3% hydrogen peroxide for 20 min in dark. Further, the sections were blocked with 1% fetal bovine serum for 30 min at RT followed by overnight incubation in primary antibody (HSP60 at 1:200; Cell Signaling Technology, USA, and CD68 at 1:100; Dako, Agilant, USA) at 4 °C in humidified chamber. After washing with PBS, sections were incubated with horseradish peroxidase (HRP)-linked secondary antibody (Dako, Agilant, USA) for 1 h at RT. Thereafter, sections were washed thoroughly with PBS and DAB (3,3’-diaminobenzidine tetrahydrochloride) substrate (Dako, Agilant, USA) was added followed by counter-staining with hematoxylin. Sections were observed under Leica DMRB microscope (Leica Camera Inc., Germany) and images were captured. Quantification of positively stained regions was carried out using Fiji software (ImageJ, NIH, Bethesda, USA) (Schindelin et al., 2012).

RNA isolation and quantitative RT-PCR

Total RNA was isolated by homogenizing the tissue in Trizol reagent (Invitrogen, Thermo Fisher Scientific, USA) according to the manufacturer’s protocol. One microgram of RNA was reverse transcribed to cDNA using iScript cDNA synthesis kit (Bio-Rad Laboratories, USA). The cDNA was used for quantitative PCR analysis using Power Up SYBR Green Master Mix (Thermo Fisher Scientific, USA) in QuantStudio-3 Real-Time PCR System (Applied Biosystems, Thermo Fisher Scientific, USA). Expression levels were analyzed using 2−∆∆CT method using GAPDH as endogenous control. Primer sequences specific for target mRNAs are listed in Table 1.

Table 1 Primer sequences for quantitative PCR

Immunoblotting

For extracting total protein lysate, tissue was homogenized in RIPA buffer (50 mM tris (pH 8.0), 150 mM NaCl, 0.5% sodium deoxycholate, 0.1% sodium dodecyl sulfate, 1% triton-X-100) containing protease inhibitor cocktail (Sigma-Aldrich, USA) and 1 mM PMSF, followed by incubation at 4 °C for 2 h. The lysate was centrifuged at 10,000 rpm at 4 °C for 20 min and resultant supernatant was subjected to protein estimation using Bio-Rad protein assay dye reagent (Bio-Rad Laboratories, USA). Twenty-five micrograms of protein was separated by SDS-PAGE and transferred onto PVDF membrane using Trans-Blot Turbo Transfer System (Bio-Rad Laboratories, USA). Membrane was blocked using 3% bovine serum albumin in Tris-buffered saline (TBS) for 1 h at RT, followed by overnight incubation in anti-HSP60 (1:750; Cell Signaling Technology, USA) and anti-β-actin antibodies (1:1000; Invitrogen, Thermo Fisher Scientific, USA) at 4 °C. Thereafter, the membrane was probed with HRP-labeled anti-rabbit secondary antibody (1:2000; Cell Signaling Technology, USA) for 1 h at RT. Expression of the immune-reactive proteins was detected using ClarityTM Western ECL Substrate (Bio-Rad Laboratories, USA) and chemiluminescence was recorded using iBright CL1000 Imaging Station (Invitrogen, Thermo Fisher Scientific, USA).

Statistical analysis

All the statistical analysis was carried out using GraphPad Prism 6.0. Differences between groups were compared by two-way ANOVA followed by Tukey’s multiple comparison test. Results were expressed as mean ± S.E.M. Differences were considered statistically significant at *P ≤ 0.05, **P ≤ 0.01, and ***P ≤ 0.001.

Results

HFHF and PMCD mediated alterations in body weight, food intake, and serum lipid profile

C57BL/6J mice were subjected to high fat high fructose (HFHF) diet, phase advance phase delay in photoperiod mediated chronodisruption (PMCD), and a combination of both variants (HFHF+PMCD). HFHF fed mice recorded significant increment in body weight and decrement in food intake as compared to control. PMCD group did not record any change in the said parameters and their values were comparable to that of control. HFHF+PMCD group recorded increment in body weight and decrement in food intake that was comparable to HFHF group (Fig. 2a, b). Parameters of the serum lipid profile viz. TG, TC, VLDL, LDL-Chol, and LDL-Chol-to-HDL-Chol ratio were significantly elevated in HFHF and HFHF+PMCD groups. PMCD group recorded significant increment in TG, VLDL, and LDL-Chol-to-HDL-Chol ratio as compared to control, whereas HDL-Chol levels recorded a marked decrement in all the groups wherein the decrement was most significant in PMCD group (Fig. 2c–h).

Fig. 2
figure2

Body weight gain, food intake, and serum lipid profiles of mice. C57BL/6J mice were fed with HFHF diet and/or subjected to PMCD. a Body weight gain and b food intake were recorded. Also, serum titers of c triglycerides (TG), d total cholesterol (TC), e very low density lipoprotein (VLDL), f low density lipoprotein-cholesterol (LDL-Chol), g high density lipoprotein-cholesterol (HDL-Chol), and h LDL-Chol/HDL-Chol ratio were assayed. Mean ± SEM (n = 6 for control, n = 10 for experimental groups). *P < 0.05, **P < 0.01, ***P < 0.001 vs control; ##P < 0.01, ###P < 0.001 vs HFHF; ++P < 0.001, +++P < 0.001 vs PMCD. ns, non-significant

HFHF and PMCD induces vascular remodeling in thoracic aorta

Microscopic evaluation of HXE stained sections of thoracic aorta revealed structural remodeling in intimal and medial regions in HFHF, PMCD, and HFHF+PMCD groups; the changes being most prominent in the PMCD group (Fig. 3a). The intima-media thickness (IMT) and luminal area of thoracic aorta showed increment in all the three groups with maximum significance recorded in the PMCD group (Fig. 3b, c). The collagen content recorded significant increments in all the three groups (Fig. 3e), whereas the collagen-to-elastin ratio recorded significant increments in the PMCD and HFHF+PMCD groups and an apparent, non-significant increase in the HFHF group (Fig. 3f). This parameter was assessed on the basis of thickening of the outer collagen observed in the picrosirius-stained sections (Fig. 3d). Auto-fluorescence of elastin in thoracic aorta of experimental mice showed derangement in all the groups and with more prominence in the PMCD group (Fig. 3g). Increased number of elastin breaks were counted in all the treatment groups with highest value recorded in PMCD group (Fig. 3h).

Fig. 3
figure3

Pro-atherogenic remodeling in thoracic aorta. a Sections of thoracic aorta were stained with HXE and images (Scale bar = 50 μm) were used for morphometric analysis of b intima-media thickness (IMT) and c lumen area. d Representative images of sections stained with picrosirius red (scale bar = 50 μm) were subjected to quantification of e collagen content relative to the total vascular area and f collagen-to-elastin ratio as a measure of arterial stiffness. g Sections were analyzed for elastin auto-fluorescence (scale bar = 50 μm; red arrows indicate breaks) and h the number of breaks/fragments in elastin laminae were counted. (i) Control, (ii) HFHF, (iii) PMCD, and (iv) HFHF+PMCD. Mean ± SEM (n = 6). *P < 0.05, **P < 0.01, ***P < 0.001 vs control; ##P < 0.01, ###P < 0.001 vs HFHF; ++P < 0.001, +++P < 0.001 vs PMCD. ns, non-significant

HFHF and PMCD induces endothelial dysfunction and atherogenic changes in thoracic aorta

Endothelial nitric oxide synthase (eNOS) is a key marker for endothelial function and feeding with HFHF diet alone could induce only moderate (non-significant) decrement in eNOS mRNA. The decrement was significant in PMCD and HFHF+PMCD groups (Fig. 4a). Markers for endothelial activation and macrophage recruitment, viz. MCP-1, VCAM-1, and ICAM-1 were assessed in thoracic aorta. mRNA levels of the said genes were significantly higher in HFHF, PMCD, and HFHF+PMCD groups (Fig. 4b). Immunolocalization of CD68 (macrophage marker) was significantly elevated in HFHF, PMCD, and HFHF+PMCD groups as evidenced by prominent positive staining of thoracic aorta (Fig. 4c, d). Overall, the said changes were more prominent in PMCD group.

Fig. 4
figure4

Endothelial dysfunction and activation in thoracic aorta. Thoracic aorta were subjected to quantitative RT-PCR of a eNOS, b MCP-1, c VCAM-1, and d ICAM-1 mRNAs (n = 3). e Sections of thoracic aorta of (i) control, (ii) HFHF, (iii) PMCD, and (iv) HFHF+PMCD groups were immunostained for CD68 (macrophage marker) (scale bar = 50 μm; black arrows indicate CD68+ areas), and d quantification of the positive areas was carried out using Image J (n = 6). Mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001 vs control, #P < 0.05, ##P < 0.01, ###P < 0.001 vs HFHF, ++P < 0.001, +++P < 0.001 vs PMCD. ns, non-significant

HFHF and PMCD mediated upregulation of HSP60 in thoracic aorta

Sections of thoracic aorta of HFHF, PMCD, and HFHF+PMCD groups stained with anti-HSP60 antibody showed prominent positive immunostaining in all the three groups (Fig. 5a). Quantitative indices of the same were found to be significant (Fig. 5b). Further, immunoblots of HSP60 in thoracic aorta of the said groups showed similar trend of increment, but the values were non-significant in HFHF and PMCD+HFHF groups (Fig. 5c).

Fig. 5
figure5

HSP60 expression in thoracic aorta. a Sections of thoracic aorta of (i) control, (ii) HFHF, (iii) PMCD, and (iv) HFHF+PMCD groups were subjected to immunohistochemical staining of HSP60 (scale bar = 50 μm) and b positive stained regions were quantified by image J (n = 6). c HSP60 expression in thoracic aorta was also assessed by immunoblotting and the same was quantified by densitometry (n = 3). Mean ± SEM. *P < 0.05, **P < 0.01 vs control, +P < 0.05 vs PMCD. ns, non-significant

Discussion

The regulatory role of circadian clock system is well established in a number of physiological processes including pathophysiological changes in human diseases. Also, subtle variations in the compositions of a high fat diet have been implicated in atherosclerosis with varying degrees of pathophysiological manifestations (Getz & Reardon, 2006; Lang, Hasselwander, Li, & Xia, 2019; Ning et al., 2015; Santana et al., 2014; Schreyer, Wilson, & LeBoeuf, 1998). However, development of cardiovascular ailments in normolipidemic condition has been implied to circadian dysregulation-induced physiological perturbations that lack clarity. In our study, the atherogenic changes resulting due to photoperiodic manipulations induced chronodisruption has been put to detailed investigation and the results have been compared with healthy (control) and HFHF diet fed C57BL/6J mice (HFHF). Also, HFHF diet fed mice subjected to circadian dysregulation (HFHF+PMCD) has been investigated for atherogenic pathophysiology.

Investigation of lipid profile of control and experimental groups revealed that the HFHF has a dominating presence in HFHF+PMCD group as the circulating titres of TG, TC, VLDL, and LDL-Chol were comparable in both the groups. However, the observed significant increment in TG and VLDL, and significant decrement in HDL-Chol are the stand-out features of the photoperiodic manipulation induced chronodisruption. HDL-Chol has been extensively reported for its physiological relevance in lipid homeostasis via reverse cholesterol transport (Marques et al., 2018). In our study, though TC and LDL-Chol levels did not show significant increment in PMCD group, significant decrement in HDL-Chol forms the basis of pro-atherogenic manifestations observed herein. These observations are in agreement with a cross-sectional study conducted in Sweden that correlated shift work with increased triglycerides and decreased HDL-cholesterol levels (Karlsson, Knutsson, & Lindahl, 2001).

Research reports on atherogenic diet fed mice/rats and high fat diet fed C57BL/6J mice have reported elevated lipid profiles and varying degrees of atherogenic changes in thoracic aorta (Cai, Miao, Xie, Lu, & Su, 2005; Santana et al., 2014). Also, previous studies in our laboratory had shown atherogenic diet induced derangement in thoracic media and intima layers (Jadeja, Thounaojam, Jain, Devkar, & Ramachandran, 2012; Patel, Desai, Gajaria, Devkar, & Ramachandran, 2013; Thounaojam, Jadeja, Salunke, Devkar, & Ramachandran, 2012). Similar changes were observed in the present study following feeding of HFHF diet wherein significant increment in IMT and lumen area corroborates our findings. Exposure of HFHF fed mice to photoperiodic manipulation induced chronodisruption also showed a similar remodeling of thoracic aorta. However, the said changes in thoracic aorta have not been reported in conditions of experimentally induced chronodisruption in mice fed with laboratory chow diet. Derangement of collagen and elastin fibers are the key events during atherogenic vascular remodeling and have been reported in our previous studies (Jadeja et al., 2012; Thounaojam et al., 2012) and in thoracic aorta of HFHF diet fed mice in both HFHF and HFHF+PMCD groups. However, pro-atherogenic vascular remodeling observed in thoracic aorta of PMCD group is a significant finding because these mice were subjected to photoperiodic phase advance and phase delay along with laboratory chow diet. Photoperiodic regimes of Schilperoort et al. (2020) had resulted in aggravation of atherosclerosis in ApoE*3-Leiden.CETP mice, but the mice fed were maintained on a Western-type diet. Another study by Anea et al. (2009) had reported pro-atherogenic vascular remodeling in Bmal1 knockout and Clock mutant mice maintained in constant darkness but these mice are naturally hyperlipidemic. In this regard, our study provides prima facie evidence on the role of photoperiodic manipulation induced chronodisruption as a causative agent for atherosclerosis without feeding atherogenic/high fat diet.

Pointing evidences on pro-atherogenic changes were obtained in the form of significant decrement in eNOS and significantly elevated atherogenic markers (MCP-1, VCAM-1, and ICAM-1) and macrophage marker (CD68) that confirmed endothelial dysfunction and subsequent atherogenic changes in all three experimental groups. These set of observations are in agreement with reports on high fat diet/atherogenic diet mediated induction of atherosclerosis (Jadeja et al., 2012; Lang et al., 2019; Thounaojam et al., 2012). Enhanced monocyte recruitment in lesions of ApoE*3-Lesion.CETP mice subjected to photoperiodic alterations has been reported, but diet induced hyperlipidemia was not ruled out as a contributing factor (Schilperoort et al., 2020). Herein, the aggravated response observed in PMCD group in terms of macrophage infiltration further supports the atherogenic progression in light of photoperiodic manipulation induced chronodisruption even in absence of dietary atherogenic stimuli.

Expression of cell adhesion molecules in pro-atherogenic vascular endothelium has been associated with HSP60 upregulation (Seitz et al., 1996) and our observations are in agreement with these reports. HSP60 upregulation suggests elevated levels of physiological stress in thoracic aorta (Hochleitner et al., 2000) that is comparable with smokers and hypertensive patients without conditions of hypercholesterolemia (Almanzar et al., 2012). Herein, we hypothesize that the pro-atherogenic changes observed in PMCD mice in spite of near normal levels of TC and LDL-Chol are attributable to photoperiod mediated stress and upregulation of HSP60 in thoracic aorta coupled with significantly low levels of HDL-Chol.

Taken together, our study highlights the role of HSP60 in inducing PMCD mediated pro-atherogenic changes, but a combination of HFHF and PMCD (HFHF+PMCD) does not result in synergistic symptoms. Overall, the findings hint at a possible underlying mechanism of atherosclerosis in normolipidemic patients.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Abbreviations

HSP60:

Heat shock protein 60

HFHF:

High fat high fructose

PMCD:

Photoperiodic manipulation induced chronodisruption

References

  1. Almanzar, G., Ollinger, R., Leuenberger, J., Onestingel, E., Rantner, B., Zehm, S., … Wick, G. (2012). Autoreactive HSP60 epitope-specific T-cells in early human atherosclerotic lesions. Journal of Autoimmunity, 39, 441–450.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  2. Amberger, A., Maczek, C., Jurgens, G., Michaelis, D., Schett, G., Trieb, K., … Wick, G. (1997). Co-expression of ICAM-1, VCAM-1, ELAM-1 and Hsp60 in human arterial and venous endothelial cells in response to cytokines and oxidized low-density lipoproteins. Cell Stress & Chaperones, 2, 94–103.

    CAS  Article  Google Scholar 

  3. Anea, C. B., Zhang, M., Stepp, D. W., Simkins, G. B., Reed, G., Fulton, D. J., & Rudic, R. D. (2009). Vascular disease in mice with a dysfunctional circadian clock. Circulation, 119, 1510–1517.

    PubMed  PubMed Central  Article  Google Scholar 

  4. Borges, L. F., Taboga, S. R., & Gutierrez, P. S. (2005). Simultaneous observation of collagen and elastin in normal and pathological tissues: Analysis of Sirius-red-stained sections by fluorescence microscopy. Cell and Tissue Research, 320, 551–552.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  5. Cai, G. J., Miao, C. Y., Xie, H. H., Lu, L. H., & Su, D. F. (2005). Arterial baroreflex dysfunction promotes atherosclerosis in rats. Atherosclerosis, 183, 41–47.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  6. Fernandez-Friera, L., Fuster, V., Lopez-Melgar, B., Oliva, B., Garcia-Ruiz, J. M., Mendiguren, J., … Sanz, J. (2017). Normal LDL-cholesterol levels are associated with subclinical atherosclerosis in the absence of risk factors. Journal of the American College of Cardiology, 70, 2979–2991.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  7. Getz, G. S., & Reardon, C. A. (2006). Diet and murine atherosclerosis. Arteriosclerosis, Thrombosis, and Vascular Biology, 26, 242–249.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  8. Grundtman, C., & Wick, G. (2011). The autoimmune concept of atherosclerosis. Current Opinion in Lipidology, 22, 327–334.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  9. Hermansson, J., Boggild, H., Hallqvist, J., Karlsson, B., Knutsson, A., Nilsson, T., … Gillander Gadin, K. (2019). Interaction between shift work and established coronary risk factors. International Journal of Occupational and Environmental Medicine, 10, 57–65.

    Article  Google Scholar 

  10. Hochleitner, B. W., Hochleitner, E. O., Obrist, P., Eberl, T., Amberger, A., Xu, Q., … Wick, G. (2000). Fluid shear stress induces heat shock protein 60 expression in endothelial cells in vitro and in vivo. Arteriosclerosis, Thrombosis, and Vascular Biology, 20, 617–623.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  11. Jadeja, R. N., Thounaojam, M. C., Jain, M., Devkar, R. V., & Ramachandran, A. V. (2012). Clerodendron glandulosum.Coleb leaf extract attenuates in vitro macrophage differentiation and expression of VCAM-1 and P-selectin in thoracic aorta of atherogenic diet fed rats. Immunopharmacology and Immunotoxicology, 34, 443–453.

    PubMed  Article  PubMed Central  Google Scholar 

  12. Jakic, B., Buszko, M., Cappellano, G., & Wick, G. (2017). Elevated sodium leads to the increased expression of HSP60 and induces apoptosis in HUVECs. PLoS One, 12, e0179383.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  13. Jankowiak, S., Backe, E., Liebers, F., Schulz, A., Hegewald, J., Garthus-Niegel, S., … Latza, U. (2016). Current and cumulative night shift work and subclinical atherosclerosis: Results of the Gutenberg health study. International Archives of Occupational and Environmental Health, 89, 1169–1182.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  14. Karlsson, B., Knutsson, A., & Lindahl, B. (2001). Is there an association between shift work and having a metabolic syndrome? Results from a population based study of 27,485 people. Occupational and Environmental Medicine, 58, 747–752.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  15. Kettner, N. M., Mayo, S. A., Hua, J., Lee, C., Moore, D. D., & Fu, L. (2015). Circadian dysfunction induces leptin resistance in mice. Cell Metabolism, 22, 448–459.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  16. Knoflach, M., Kiechl, S., Kind, M., Said, M., Sief, R., Gisinger, M., … Wick, G. (2003). Cardiovascular risk factors and atherosclerosis in young males: ARMY study (atherosclerosis risk-factors in male youngsters). Circulation, 108, 1064–1069.

    PubMed  Article  Google Scholar 

  17. Knoflach, M., Kiechl, S., Penz, D., Zangerle, A., Schmidauer, C., Rossmann, A., … Wick, G. (2009). Cardiovascular risk factors and atherosclerosis in young women: Atherosclerosis risk factors in female youngsters (ARFY study). Stroke, 40, 1063–1069.

    CAS  PubMed  Article  Google Scholar 

  18. Knutsson, A., Hammar, N., & Karlsson, B. (2004). Shift workers' mortality scrutinized. Chronobiology International, 21, 1049–1053.

    PubMed  Article  Google Scholar 

  19. Kreutmayer, S., Csordas, A., Kern, J., Maass, V., Almanzar, G., Offterdinger, M., … Wick, G. (2013). Chlamydia pneumoniae infection acts as an endothelial stressor with the potential to initiate the earliest heat shock protein 60-dependent inflammatory stage of atherosclerosis. Cell Stress & Chaperones, 18, 259–268.

    CAS  Article  Google Scholar 

  20. Kreutmayer, S. B., Messner, B., Knoflach, M., Henderson, B., Niederegger, H., Bock, G., … Bernhard, D. (2011). Dynamics of heat shock protein 60 in endothelial cells exposed to cigarette smoke extract. Journal of Molecular and Cellular Cardiology, 51, 777–780.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  21. Lang, P., Hasselwander, S., Li, H., & Xia, N. (2019). Effects of different diets used in diet-induced obesity models on insulin resistance and vascular dysfunction in C57BL/6 mice. Scientific Reports, 9, 19556.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  22. Marques, L. R., Diniz, T. A., Antunes, B. M., Rossi, F. E., Caperuto, E. C., Lira, F. S., & Goncalves, D. C. (2018). Reverse cholesterol transport: Molecular mechanisms and the non-medical approach to enhance HDL cholesterol. Frontiers in Physiology, 9, 526.

    PubMed  PubMed Central  Article  Google Scholar 

  23. Muller, J. E., Stone, P. H., Turi, Z. G., Rutherford, J. D., Czeisler, C. A., Parker, C., et al. (1985). Circadian variation in the frequency of onset of acute myocardial infarction. The New England Journal of Medicine, 313, 1315–1322.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  24. Ning, B., Wang, X., Yu, Y., Waqar, A. B., Yu, Q., Koike, T., … Fan, J. (2015). High-fructose and high-fat diet-induced insulin resistance enhances atherosclerosis in Watanabe heritable hyperlipidemic rabbits. Nutrition & Metabolism (London), 12, 30.

    Article  CAS  Google Scholar 

  25. Patel, D., Desai, S., Gajaria, T., Devkar, R., & Ramachandran, A. V. (2013). Coriandrum sativum L. seed extract mitigates lipotoxicity in RAW 264.7 cells and prevents atherogenic changes in rats. EXCLI Journal, 12, 313–334.

    PubMed  PubMed Central  Google Scholar 

  26. Ridker, P. M., Danielson, E., Fonseca, F. A., Genest, J., Gotto Jr., A. M., Kastelein, J. J., … Group, J.S (2008). Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. The New England Journal of Medicine, 359, 2195–2207.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  27. Santana, A. B., de Souza Oliveira, T. C., Bianconi, B. L., Barauna, V. G., Santos, E. W., Alves, T. P., … Lacchini, S. (2014). Effect of high-fat diet upon inflammatory markers and aortic stiffening in mice. BioMed Research International, 2014, 914102.

    PubMed  PubMed Central  Article  Google Scholar 

  28. Sawada, H., & Daugherty, A. (2018). Quantification of elastin fragmentation in the ascending aorta.

    Google Scholar 

  29. Scheer, F. A., Hilton, M. F., Mantzoros, C. S., & Shea, S. A. (2009). Adverse metabolic and cardiovascular consequences of circadian misalignment. Proceedings of the National Academy of Sciences of the United States of America, 106, 4453–4458.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  30. Schilperoort, M., van den Berg, R., Bosmans, L. A., van Os, B. W., Dolle, M. E. T., Smits, N. A. M., … Kooijman, S. (2020). Disruption of circadian rhythm by alternating light-dark cycles aggravates atherosclerosis development in APOE*3-Leiden.CETP mice. Journal of Pineal Research, 68, e12614.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  31. Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., … Cardona, A. (2012). Fiji: An open-source platform for biological-image analysis. Nature Methods, 9, 676–682.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  32. Schreyer, S. A., Wilson, D. L., & LeBoeuf, R. C. (1998). C57BL/6 mice fed high fat diets as models for diabetes-accelerated atherosclerosis. Atherosclerosis, 136, 17–24.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  33. Seitz, C. S., Kleindienst, R., Xu, Q., & Wick, G. (1996). Coexpression of heat-shock protein 60 and intercellular-adhesion molecule-1 is related to increased adhesion of monocytes and T cells to aortic endothelium of rats in response to endotoxin. Laboratory Investigation, 74, 241–252.

    CAS  PubMed  PubMed Central  Google Scholar 

  34. Sniderman, A., Shapiro, S., Marpole, D., Skinner, B., Teng, B., & Kwiterovich Jr., P. O. (1980). Association of coronary atherosclerosis with hyperapobetalipoproteinemia [increased protein but normal cholesterol levels in human plasma low density (beta) lipoproteins]. Proceedings of the National Academy of Sciences of the United States of America, 77, 604–608.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  35. Somanath, P. R., Podrez, E. A., Chen, J., Ma, Y., Marchant, K., Antoch, M., & Byzova, T. V. (2011). Deficiency in core circadian protein Bmal1 is associated with a prothrombotic and vascular phenotype. Journal of Cellular Physiology, 226, 132–140.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  36. Thounaojam, M. C., Jadeja, R. N., Salunke, S. P., Devkar, R. V., & Ramachandran, A. V. (2012). Sida rhomboidea.Roxb aqueous extract down-regulates in vivo expression of vascular cell adhesion molecules in atherogenic rats and inhibits in vitro macrophage differentiation and foam cell formation. Immunopharmacology and Immunotoxicology, 34, 832–843.

    PubMed  Article  PubMed Central  Google Scholar 

  37. Vogel, B., Siebert, H., Hofmann, U., & Frantz, S. (2015). Determination of collagen content within picrosirius red stained paraffin-embedded tissue sections using fluorescence microscopy. MethodsX, 2, 124–134.

    PubMed  PubMed Central  Article  Google Scholar 

  38. Willich, S. N. (1990). Epidemiologic studies demonstrating increased morning incidence of sudden cardiac death. The American Journal of Cardiology, 66, 15G–17G.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  39. Xu, Q., Kiechl, S., Mayr, M., Metzler, B., Egger, G., Oberhollenzer, F., … Wick, G. (1999). Association of serum antibodies to heat-shock protein 65 with carotid atherosclerosis : Clinical significance determined in a follow-up study. Circulation, 100, 1169–1174.

    CAS  PubMed  Article  Google Scholar 

  40. Xu, Q., Schett, G., Perschinka, H., Mayr, M., Egger, G., Oberhollenzer, F., … Wick, G. (2000). Serum soluble heat shock protein 60 is elevated in subjects with atherosclerosis in a general population. Circulation, 102, 14–20.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  41. Xu, Q., Willeit, J., Marosi, M., Kleindienst, R., Oberhollenzer, F., Kiechl, S., … Wick, G. (1993). Association of serum antibodies to heat-shock protein 65 with carotid atherosclerosis. Lancet, 341, 255–259.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  42. Zhao, Y., Zhang, C., Wei, X., Li, P., Cui, Y., Qin, Y., … Gao, Y. (2015). Heat shock protein 60 stimulates the migration of vascular smooth muscle cells via toll-like receptor 4 and ERK MAPK activation. Scientific Reports, 5, 15352.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

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Acknowledgements

KS has acknowledged University Grant Commission (UGC), New Delhi, India, for providing fellowship (UGC-RGNF). Technical helps in various capacities rendered by Prof. Rajesh Singh (Biochemistry), Prof. Vihas Vasu (Zoology), and Dr. Kishore Rajput (Botany), MSU Baroda, are duly acknowledged.

Funding

The work was funded under Core Research Grant (SERB EMR/2015/002001) of Science and Engineering Research Board (SERB), New Delhi, India, to RD.

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K.S. and R.D. conceptualized the idea and designed the study. K.S., A.J., and A.V. performed in vivo experimentation. K.S. analyzed the data, whereas K.S. and R.D. interpreted the data and drafted the manuscript. All authors approve the final version of the manuscript.

Corresponding author

Correspondence to Ranjitsinh Devkar.

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The animal experiment protocol (MSU-Z/IAEC/2/09-2017) was approved by the Institutional Animal Ethical Committee (IAEC), Department of Zoology, The Maharaja Sayajirao University of Baroda, and the experiments were conducted in accordance with the guidelines of the Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA).

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Shirsath, K., Joshi, A., Vohra, A. et al. Chronic photoperiodic manipulation induced chronodisruption upregulates HSP60 during early pro-atherogenic remodeling in thoracic aorta of C57BL/6J mice. JoBAZ 82, 9 (2021). https://doi.org/10.1186/s41936-021-00205-2

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Keywords

  • Atherosclerosis
  • HSP60
  • Chronodisruption
  • Vascular remodeling
  • High fat high fructose diet
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