Circulating

Impaired Glc tolerance and hyperinsulinemia are a hallmark of type 2 diabetes (T2D) and are associated with an altered innate and adaptive immune response. In this study, we used a high-fat diet (HFD)-induced model of pre-diabetes to explore the pathological implications of altered innate lymphoid c...

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Autores principales: Vuyolwethu Mxinwa, Phiwayinkosi V. Dludla, Tawanda M. Nyambuya, Bongani B. Nkambule
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Lenguaje:EN
Publicado: SAGE Publishing 2021
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Acceso en línea:https://doaj.org/article/bed6630e01ff4507adaef7999e0f2462
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spelling oai:doaj.org-article:bed6630e01ff4507adaef7999e0f24622021-12-02T07:35:16ZCirculating1753-42591753-426710.1177/17534259211053634https://doaj.org/article/bed6630e01ff4507adaef7999e0f24622021-10-01T00:00:00Zhttps://doi.org/10.1177/17534259211053634https://doaj.org/toc/1753-4259https://doaj.org/toc/1753-4267Impaired Glc tolerance and hyperinsulinemia are a hallmark of type 2 diabetes (T2D) and are associated with an altered innate and adaptive immune response. In this study, we used a high-fat diet (HFD)-induced model of pre-diabetes to explore the pathological implications of altered innate lymphoid cell (ILC) profiles in a state of impaired Glc tolerance. Sixteen male C57BL/6 mice were randomized to receive two experimental diets ( n  = 8 per group), low-fat (LFD), and HFD for 8–13 wk. We evaluated the levels of circulating innate lymphoid cells and their respective cytokines following HFD-feeding. The HFD group had impaired Glc tolerance, elevated insulin levels, and increased total cholesterol levels. Notably, the levels of circulating ILC1s were elevated following 13 wk of HFD-feeding. Moreover, the levels of TNF-α were decreased, but there were no changes in IFN-γ levels. Lastly, the levels of circulating ILC2s and ILC3s were comparable between the HFD and LFD group. The findings demonstrated that short-term HFD-feeding increases postprandial blood Glc, total cholesterol and insulin levels. However, the metabolic changes did not alter ILC2 and ILC3 levels and their respective cytokine profiles.Vuyolwethu MxinwaPhiwayinkosi V. DludlaTawanda M. NyambuyaBongani B. NkambuleSAGE PublishingarticleImmunologic diseases. AllergyRC581-607ENInnate Immunity, Vol 27 (2021)
institution DOAJ
collection DOAJ
language EN
topic Immunologic diseases. Allergy
RC581-607
spellingShingle Immunologic diseases. Allergy
RC581-607
Vuyolwethu Mxinwa
Phiwayinkosi V. Dludla
Tawanda M. Nyambuya
Bongani B. Nkambule
Circulating
description Impaired Glc tolerance and hyperinsulinemia are a hallmark of type 2 diabetes (T2D) and are associated with an altered innate and adaptive immune response. In this study, we used a high-fat diet (HFD)-induced model of pre-diabetes to explore the pathological implications of altered innate lymphoid cell (ILC) profiles in a state of impaired Glc tolerance. Sixteen male C57BL/6 mice were randomized to receive two experimental diets ( n  = 8 per group), low-fat (LFD), and HFD for 8–13 wk. We evaluated the levels of circulating innate lymphoid cells and their respective cytokines following HFD-feeding. The HFD group had impaired Glc tolerance, elevated insulin levels, and increased total cholesterol levels. Notably, the levels of circulating ILC1s were elevated following 13 wk of HFD-feeding. Moreover, the levels of TNF-α were decreased, but there were no changes in IFN-γ levels. Lastly, the levels of circulating ILC2s and ILC3s were comparable between the HFD and LFD group. The findings demonstrated that short-term HFD-feeding increases postprandial blood Glc, total cholesterol and insulin levels. However, the metabolic changes did not alter ILC2 and ILC3 levels and their respective cytokine profiles.
format article
author Vuyolwethu Mxinwa
Phiwayinkosi V. Dludla
Tawanda M. Nyambuya
Bongani B. Nkambule
author_facet Vuyolwethu Mxinwa
Phiwayinkosi V. Dludla
Tawanda M. Nyambuya
Bongani B. Nkambule
author_sort Vuyolwethu Mxinwa
title Circulating
title_short Circulating
title_full Circulating
title_fullStr Circulating
title_full_unstemmed Circulating
title_sort circulating
publisher SAGE Publishing
publishDate 2021
url https://doaj.org/article/bed6630e01ff4507adaef7999e0f2462
work_keys_str_mv AT vuyolwethumxinwa circulating
AT phiwayinkosivdludla circulating
AT tawandamnyambuya circulating
AT bonganibnkambule circulating
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