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Circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet
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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762092/ https://www.ncbi.nlm.nih.gov/pubmed/34787473 http://dx.doi.org/10.1177/17534259211053634 |
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author | Mxinwa, Vuyolwethu Dludla, Phiwayinkosi V. Nyambuya, Tawanda M. Nkambule, Bongani B. |
author_facet | Mxinwa, Vuyolwethu Dludla, Phiwayinkosi V. Nyambuya, Tawanda M. Nkambule, Bongani B. |
author_sort | Mxinwa, Vuyolwethu |
collection | PubMed |
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 | Online Article Text |
id | pubmed-8762092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-87620922022-01-18 Circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet Mxinwa, Vuyolwethu Dludla, Phiwayinkosi V. Nyambuya, Tawanda M. Nkambule, Bongani B. Innate Immun Original Articles 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. SAGE Publications 2021-11-17 2021-10 /pmc/articles/PMC8762092/ /pubmed/34787473 http://dx.doi.org/10.1177/17534259211053634 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Mxinwa, Vuyolwethu Dludla, Phiwayinkosi V. Nyambuya, Tawanda M. Nkambule, Bongani B. Circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet |
title | Circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet |
title_full | Circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet |
title_fullStr | Circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet |
title_full_unstemmed | Circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet |
title_short | Circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet |
title_sort | circulating innate lymphoid cell subtypes and altered cytokine profiles following an atherogenic high-fat diet |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762092/ https://www.ncbi.nlm.nih.gov/pubmed/34787473 http://dx.doi.org/10.1177/17534259211053634 |
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