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Lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in MRL/lpr mice

OBJECTIVE: SLE is an autoimmune disease characterised by persistent inflammation and autoantibody production. Genetic predisposition and environmental factors such as a high-fat diet (HFD) may contribute to lupus development. However, the immune cell profile and gender difference in response to HFD...

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Autores principales: Zhang, Xin, Meng, Juan, Shi, Xuhua, Quinet, Robert James, Davis, William, Zakem, Jerald, Keshavamurthy, Chandana, Patel, Ronak, Lobo, Gitanjali, Hellmers, Linh, Ray, Alicia Nicole, Rivers, Laura E, Ali, Hiba, Posas-Mendoza, Therese, Hille, Chad, You, Zongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106072/
https://www.ncbi.nlm.nih.gov/pubmed/37041033
http://dx.doi.org/10.1136/lupus-2023-000898
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author Zhang, Xin
Meng, Juan
Shi, Xuhua
Quinet, Robert James
Davis, William
Zakem, Jerald
Keshavamurthy, Chandana
Patel, Ronak
Lobo, Gitanjali
Hellmers, Linh
Ray, Alicia Nicole
Rivers, Laura E
Ali, Hiba
Posas-Mendoza, Therese
Hille, Chad
You, Zongbing
author_facet Zhang, Xin
Meng, Juan
Shi, Xuhua
Quinet, Robert James
Davis, William
Zakem, Jerald
Keshavamurthy, Chandana
Patel, Ronak
Lobo, Gitanjali
Hellmers, Linh
Ray, Alicia Nicole
Rivers, Laura E
Ali, Hiba
Posas-Mendoza, Therese
Hille, Chad
You, Zongbing
author_sort Zhang, Xin
collection PubMed
description OBJECTIVE: SLE is an autoimmune disease characterised by persistent inflammation and autoantibody production. Genetic predisposition and environmental factors such as a high-fat diet (HFD) may contribute to lupus development. However, the immune cell profile and gender difference in response to HFD in lupus have not been reported. Here we investigated the impact of HFD on lupus pathogenesis and autoimmunity using lupus-prone mice. METHODS: Thirty male and 30 female MRL/lymphoproliferation (lpr) mice were fed with regular diet (RD) or HFD. Body weights were recorded weekly. SLE progression was monitored by skin lesion, urine protein, titres of antidouble-strand DNA (dsDNA) and ANA. At week 14, kidney and skin tissue sections were stained with H&E and periodic acid–Schiff to detect histological kidney index and skin score. Splenocytes were identified by immunofluorescence staining and flow cytometry. RESULTS: HFD significantly increased body weight and lipid levels compared with RD (p<0.01). Skin lesions were observed in 55.6% of the HFD group compared with 11.1% of the RD group, with greater histopathological skin scores in the female HFD group (p<0.01). Although both male and female mice had higher serum IgG in the HFD group than in the RD group, only the male HFD group showed an increased trend in anti-dsDNA Ab and ANA titres. Kidney pathological changes in the HFD group were more severe in male mice than in female mice (p<0.05), detected by proteinuria, kidney index and glomerular cell proliferation. Significant increases of germinal centre B cells and T follicular helper cells were observed in the spleens of HFD mice (p<0.05). CONCLUSION: HFD induced an accelerated and exacerbated lupus development and autoimmunity in MRL/lpr mice. Our results parallel many known clinical lupus phenotypes and sexual dimorphism in which male patients are likelier to have a severe disease (nephritis) than female lupus patients who may have a broader range of lupus symptoms.
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spelling pubmed-101060722023-04-17 Lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in MRL/lpr mice Zhang, Xin Meng, Juan Shi, Xuhua Quinet, Robert James Davis, William Zakem, Jerald Keshavamurthy, Chandana Patel, Ronak Lobo, Gitanjali Hellmers, Linh Ray, Alicia Nicole Rivers, Laura E Ali, Hiba Posas-Mendoza, Therese Hille, Chad You, Zongbing Lupus Sci Med Animal Models OBJECTIVE: SLE is an autoimmune disease characterised by persistent inflammation and autoantibody production. Genetic predisposition and environmental factors such as a high-fat diet (HFD) may contribute to lupus development. However, the immune cell profile and gender difference in response to HFD in lupus have not been reported. Here we investigated the impact of HFD on lupus pathogenesis and autoimmunity using lupus-prone mice. METHODS: Thirty male and 30 female MRL/lymphoproliferation (lpr) mice were fed with regular diet (RD) or HFD. Body weights were recorded weekly. SLE progression was monitored by skin lesion, urine protein, titres of antidouble-strand DNA (dsDNA) and ANA. At week 14, kidney and skin tissue sections were stained with H&E and periodic acid–Schiff to detect histological kidney index and skin score. Splenocytes were identified by immunofluorescence staining and flow cytometry. RESULTS: HFD significantly increased body weight and lipid levels compared with RD (p<0.01). Skin lesions were observed in 55.6% of the HFD group compared with 11.1% of the RD group, with greater histopathological skin scores in the female HFD group (p<0.01). Although both male and female mice had higher serum IgG in the HFD group than in the RD group, only the male HFD group showed an increased trend in anti-dsDNA Ab and ANA titres. Kidney pathological changes in the HFD group were more severe in male mice than in female mice (p<0.05), detected by proteinuria, kidney index and glomerular cell proliferation. Significant increases of germinal centre B cells and T follicular helper cells were observed in the spleens of HFD mice (p<0.05). CONCLUSION: HFD induced an accelerated and exacerbated lupus development and autoimmunity in MRL/lpr mice. Our results parallel many known clinical lupus phenotypes and sexual dimorphism in which male patients are likelier to have a severe disease (nephritis) than female lupus patients who may have a broader range of lupus symptoms. BMJ Publishing Group 2023-04-11 /pmc/articles/PMC10106072/ /pubmed/37041033 http://dx.doi.org/10.1136/lupus-2023-000898 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Animal Models
Zhang, Xin
Meng, Juan
Shi, Xuhua
Quinet, Robert James
Davis, William
Zakem, Jerald
Keshavamurthy, Chandana
Patel, Ronak
Lobo, Gitanjali
Hellmers, Linh
Ray, Alicia Nicole
Rivers, Laura E
Ali, Hiba
Posas-Mendoza, Therese
Hille, Chad
You, Zongbing
Lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in MRL/lpr mice
title Lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in MRL/lpr mice
title_full Lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in MRL/lpr mice
title_fullStr Lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in MRL/lpr mice
title_full_unstemmed Lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in MRL/lpr mice
title_short Lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in MRL/lpr mice
title_sort lupus pathogenesis and autoimmunity are exacerbated by high fat diet-induced obesity in mrl/lpr mice
topic Animal Models
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106072/
https://www.ncbi.nlm.nih.gov/pubmed/37041033
http://dx.doi.org/10.1136/lupus-2023-000898
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