Mesenchymal Stem/Stromal Cells Reverse Adipose Tissue Inflammation in Pigs with Metabolic Syndrome and Renovascular Hypertension

Metabolic syndrome (MetS) is associated with low-grade inflammation, which can be exacerbated by renal artery stenosis (RAS) and renovascular hypertension, potentially worsening outcomes through pro-inflammatory cytokines. This study investigated whether mesenchymal stem/stromal cells (MSCs) could r...

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Main Authors: Alexander B. C. Krueger, Xiangyang Zhu, Sarosh Siddiqi, Emma C. Whitehead, Hui Tang, Kyra L. Jordan, Amir Lerman, Lilach O. Lerman
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Cells
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Online Access:https://www.mdpi.com/2073-4409/14/1/40
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author Alexander B. C. Krueger
Xiangyang Zhu
Sarosh Siddiqi
Emma C. Whitehead
Hui Tang
Kyra L. Jordan
Amir Lerman
Lilach O. Lerman
author_facet Alexander B. C. Krueger
Xiangyang Zhu
Sarosh Siddiqi
Emma C. Whitehead
Hui Tang
Kyra L. Jordan
Amir Lerman
Lilach O. Lerman
author_sort Alexander B. C. Krueger
collection DOAJ
description Metabolic syndrome (MetS) is associated with low-grade inflammation, which can be exacerbated by renal artery stenosis (RAS) and renovascular hypertension, potentially worsening outcomes through pro-inflammatory cytokines. This study investigated whether mesenchymal stem/stromal cells (MSCs) could reduce fat inflammation in pigs with MetS and RAS. Twenty-four pigs were divided into Lean (control), MetS, MetS + RAS, and MetS + RAS + MSCs. In the MSC-treated group, autologous adipose-derived MSCs (10<sup>7</sup> cells) were injected into the renal artery six weeks after RAS induction. After four weeks, fat volumes and inflammatory markers were assessed. MSC treatment reduced levels of pro-inflammatory cytokines (MCP-1, TNF-a, IL-6) in the renal vein blood and in perirenal fat. The MSCs also decreased fat fibrosis, restored adipocyte size, and altered adipogenesis-related gene expression, particularly in the perirenal fat. These effects were less pronounced in subcutaneous fat. The MSC therapy attenuated fat inflammation and improved metabolic outcomes in pigs with MetS + RAS, suggesting that adipose-derived MSCs may offer a promising therapeutic approach for metabolic disorders.
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spelling doaj-art-21c4ef6136f846b58798030706dd7dda2025-01-10T13:16:20ZengMDPI AGCells2073-44092025-01-011414010.3390/cells14010040Mesenchymal Stem/Stromal Cells Reverse Adipose Tissue Inflammation in Pigs with Metabolic Syndrome and Renovascular HypertensionAlexander B. C. Krueger0Xiangyang Zhu1Sarosh Siddiqi2Emma C. Whitehead3Hui Tang4Kyra L. Jordan5Amir Lerman6Lilach O. Lerman7Division of Nephrology & Hypertension, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USADivision of Nephrology & Hypertension, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USADivision of Nephrology & Hypertension, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USADivision of Nephrology & Hypertension, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USADivision of Nephrology & Hypertension, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USADivision of Nephrology & Hypertension, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USADepartment of Cardiovascular Diseases, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USADivision of Nephrology & Hypertension, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USAMetabolic syndrome (MetS) is associated with low-grade inflammation, which can be exacerbated by renal artery stenosis (RAS) and renovascular hypertension, potentially worsening outcomes through pro-inflammatory cytokines. This study investigated whether mesenchymal stem/stromal cells (MSCs) could reduce fat inflammation in pigs with MetS and RAS. Twenty-four pigs were divided into Lean (control), MetS, MetS + RAS, and MetS + RAS + MSCs. In the MSC-treated group, autologous adipose-derived MSCs (10<sup>7</sup> cells) were injected into the renal artery six weeks after RAS induction. After four weeks, fat volumes and inflammatory markers were assessed. MSC treatment reduced levels of pro-inflammatory cytokines (MCP-1, TNF-a, IL-6) in the renal vein blood and in perirenal fat. The MSCs also decreased fat fibrosis, restored adipocyte size, and altered adipogenesis-related gene expression, particularly in the perirenal fat. These effects were less pronounced in subcutaneous fat. The MSC therapy attenuated fat inflammation and improved metabolic outcomes in pigs with MetS + RAS, suggesting that adipose-derived MSCs may offer a promising therapeutic approach for metabolic disorders.https://www.mdpi.com/2073-4409/14/1/40metabolic syndromerenal artery stenosismesenchymal stem cellsinflammation
spellingShingle Alexander B. C. Krueger
Xiangyang Zhu
Sarosh Siddiqi
Emma C. Whitehead
Hui Tang
Kyra L. Jordan
Amir Lerman
Lilach O. Lerman
Mesenchymal Stem/Stromal Cells Reverse Adipose Tissue Inflammation in Pigs with Metabolic Syndrome and Renovascular Hypertension
Cells
metabolic syndrome
renal artery stenosis
mesenchymal stem cells
inflammation
title Mesenchymal Stem/Stromal Cells Reverse Adipose Tissue Inflammation in Pigs with Metabolic Syndrome and Renovascular Hypertension
title_full Mesenchymal Stem/Stromal Cells Reverse Adipose Tissue Inflammation in Pigs with Metabolic Syndrome and Renovascular Hypertension
title_fullStr Mesenchymal Stem/Stromal Cells Reverse Adipose Tissue Inflammation in Pigs with Metabolic Syndrome and Renovascular Hypertension
title_full_unstemmed Mesenchymal Stem/Stromal Cells Reverse Adipose Tissue Inflammation in Pigs with Metabolic Syndrome and Renovascular Hypertension
title_short Mesenchymal Stem/Stromal Cells Reverse Adipose Tissue Inflammation in Pigs with Metabolic Syndrome and Renovascular Hypertension
title_sort mesenchymal stem stromal cells reverse adipose tissue inflammation in pigs with metabolic syndrome and renovascular hypertension
topic metabolic syndrome
renal artery stenosis
mesenchymal stem cells
inflammation
url https://www.mdpi.com/2073-4409/14/1/40
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