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Uterine Sensitization-Associated Gene-1 in the Progression of Kidney Diseases

Uterine sensitization-associated gene-1 (USAG-1), originally identified as a secretory protein preferentially expressed in the sensitized rat endometrium, has been determined to modulate bone morphogenetic protein (BMP) and Wnt expression to play important roles in kidney disease. USAG-1 affects the...

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Detalles Bibliográficos
Autores principales: Li, Xiaohu, Yue, Wenlong, Feng, Guiwen, Li, Jinfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369194/
https://www.ncbi.nlm.nih.gov/pubmed/34414243
http://dx.doi.org/10.1155/2021/9752139
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author Li, Xiaohu
Yue, Wenlong
Feng, Guiwen
Li, Jinfeng
author_facet Li, Xiaohu
Yue, Wenlong
Feng, Guiwen
Li, Jinfeng
author_sort Li, Xiaohu
collection PubMed
description Uterine sensitization-associated gene-1 (USAG-1), originally identified as a secretory protein preferentially expressed in the sensitized rat endometrium, has been determined to modulate bone morphogenetic protein (BMP) and Wnt expression to play important roles in kidney disease. USAG-1 affects the progression of acute and chronic kidney damage and the recovery of allograft kidney function by regulating the BMP and Wnt signaling pathways. Moreover, USAG-1 has been found to be involved in the process of T cell immune response, and its ability to inhibit germinal center activity and reduce humoral immunity is of great significance for the treatment of autoimmune nephropathy and antibody-mediated rejection (AMR) after renal transplantation. This article summarizes the many advances made regarding the roles of USAG-1 in the progression of kidney disease and outlines potential treatments.
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spelling pubmed-83691942021-08-18 Uterine Sensitization-Associated Gene-1 in the Progression of Kidney Diseases Li, Xiaohu Yue, Wenlong Feng, Guiwen Li, Jinfeng J Immunol Res Review Article Uterine sensitization-associated gene-1 (USAG-1), originally identified as a secretory protein preferentially expressed in the sensitized rat endometrium, has been determined to modulate bone morphogenetic protein (BMP) and Wnt expression to play important roles in kidney disease. USAG-1 affects the progression of acute and chronic kidney damage and the recovery of allograft kidney function by regulating the BMP and Wnt signaling pathways. Moreover, USAG-1 has been found to be involved in the process of T cell immune response, and its ability to inhibit germinal center activity and reduce humoral immunity is of great significance for the treatment of autoimmune nephropathy and antibody-mediated rejection (AMR) after renal transplantation. This article summarizes the many advances made regarding the roles of USAG-1 in the progression of kidney disease and outlines potential treatments. Hindawi 2021-08-07 /pmc/articles/PMC8369194/ /pubmed/34414243 http://dx.doi.org/10.1155/2021/9752139 Text en Copyright © 2021 Xiaohu Li et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Li, Xiaohu
Yue, Wenlong
Feng, Guiwen
Li, Jinfeng
Uterine Sensitization-Associated Gene-1 in the Progression of Kidney Diseases
title Uterine Sensitization-Associated Gene-1 in the Progression of Kidney Diseases
title_full Uterine Sensitization-Associated Gene-1 in the Progression of Kidney Diseases
title_fullStr Uterine Sensitization-Associated Gene-1 in the Progression of Kidney Diseases
title_full_unstemmed Uterine Sensitization-Associated Gene-1 in the Progression of Kidney Diseases
title_short Uterine Sensitization-Associated Gene-1 in the Progression of Kidney Diseases
title_sort uterine sensitization-associated gene-1 in the progression of kidney diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369194/
https://www.ncbi.nlm.nih.gov/pubmed/34414243
http://dx.doi.org/10.1155/2021/9752139
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