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The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models
V-set Ig domain-containing 4 (VSIG4) regulates an inflammatory response and is involved in various diseases. However, the role of VSIG4 in kidney diseases is still unclear. Here, we investigated VSIG4 expression in unilateral ureteral obstruction (UUO), doxorubicin-induced kidney injury mouse, and d...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965633/ https://www.ncbi.nlm.nih.gov/pubmed/36836636 http://dx.doi.org/10.3390/life13020277 |
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author | Han, Sang Youb Ghee, Jung Yeon Cha, Jin Joo Kang, Young Sun Kim, Han Seong Hur, Dae Young Cha, Dae Ryong |
author_facet | Han, Sang Youb Ghee, Jung Yeon Cha, Jin Joo Kang, Young Sun Kim, Han Seong Hur, Dae Young Cha, Dae Ryong |
author_sort | Han, Sang Youb |
collection | PubMed |
description | V-set Ig domain-containing 4 (VSIG4) regulates an inflammatory response and is involved in various diseases. However, the role of VSIG4 in kidney diseases is still unclear. Here, we investigated VSIG4 expression in unilateral ureteral obstruction (UUO), doxorubicin-induced kidney injury mouse, and doxorubicin-induced podocyte injury models. The levels of urinary VSIG4 protein significantly increased in the UUO mice compared with that in the control. The expression of VSIG4 mRNA and protein in the UUO mice was significantly upregulated compared with that in the control. In the doxorubicin-induced kidney injury model, the levels of urinary albumin and VSIG4 for 24 h were significantly higher than those in the control mice. Notably, a significant correlation was observed between urinary levels of VSIG4 and albumin (r = 0.912, p < 0.001). Intrarenal VSIG4 mRNA and protein expression were also significantly higher in the doxorubicin-induced mice than in the control. In cultured podocytes, VSIG4 mRNA and protein expressions were significantly higher in the doxorubicin-treated groups (1.0 and 3.0 μg/mL) than in the controls at 12 and 24 h. In conclusion, VSIG4 expression was upregulated in the UUO and doxorubicin-induced kidney injury models. VSIG4 may be involved in pathogenesis and disease progression in chronic kidney disease models. |
format | Online Article Text |
id | pubmed-9965633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99656332023-02-26 The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models Han, Sang Youb Ghee, Jung Yeon Cha, Jin Joo Kang, Young Sun Kim, Han Seong Hur, Dae Young Cha, Dae Ryong Life (Basel) Communication V-set Ig domain-containing 4 (VSIG4) regulates an inflammatory response and is involved in various diseases. However, the role of VSIG4 in kidney diseases is still unclear. Here, we investigated VSIG4 expression in unilateral ureteral obstruction (UUO), doxorubicin-induced kidney injury mouse, and doxorubicin-induced podocyte injury models. The levels of urinary VSIG4 protein significantly increased in the UUO mice compared with that in the control. The expression of VSIG4 mRNA and protein in the UUO mice was significantly upregulated compared with that in the control. In the doxorubicin-induced kidney injury model, the levels of urinary albumin and VSIG4 for 24 h were significantly higher than those in the control mice. Notably, a significant correlation was observed between urinary levels of VSIG4 and albumin (r = 0.912, p < 0.001). Intrarenal VSIG4 mRNA and protein expression were also significantly higher in the doxorubicin-induced mice than in the control. In cultured podocytes, VSIG4 mRNA and protein expressions were significantly higher in the doxorubicin-treated groups (1.0 and 3.0 μg/mL) than in the controls at 12 and 24 h. In conclusion, VSIG4 expression was upregulated in the UUO and doxorubicin-induced kidney injury models. VSIG4 may be involved in pathogenesis and disease progression in chronic kidney disease models. MDPI 2023-01-19 /pmc/articles/PMC9965633/ /pubmed/36836636 http://dx.doi.org/10.3390/life13020277 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Han, Sang Youb Ghee, Jung Yeon Cha, Jin Joo Kang, Young Sun Kim, Han Seong Hur, Dae Young Cha, Dae Ryong The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models |
title | The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models |
title_full | The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models |
title_fullStr | The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models |
title_full_unstemmed | The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models |
title_short | The Role of V-Set Ig Domain-Containing 4 in Chronic Kidney Disease Models |
title_sort | role of v-set ig domain-containing 4 in chronic kidney disease models |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965633/ https://www.ncbi.nlm.nih.gov/pubmed/36836636 http://dx.doi.org/10.3390/life13020277 |
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