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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.
Afiliación
  • Han SY; Department of Internal Medicine, Inje University, Ilsan-Paik Hospital, Goyang 10380, Republic of Korea.
  • Ghee JY; Department of Internal Medicine, Korea University, Ansan Hospital, Ansan 15355, Republic of Korea.
  • Cha JJ; Department of Internal Medicine, Korea University, Ansan Hospital, Ansan 15355, Republic of Korea.
  • Kang YS; Department of Internal Medicine, Korea University, Ansan Hospital, Ansan 15355, Republic of Korea.
  • Kim HS; Department of Pathology, Inje University, Ilsan-Paik Hospital, Goyang 10380, Republic of Korea.
  • Hur DY; Department of Anatomy and Tumor Immunology, Inje University College of Medicine, Busan 47392, Republic of Korea.
  • Cha DR; Department of Internal Medicine, Korea University, Ansan Hospital, Ansan 15355, Republic of Korea.
Life (Basel) ; 13(2)2023 Jan 19.
Article en En | MEDLINE | ID: mdl-36836636
ABSTRACT
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Life (Basel) Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Life (Basel) Año: 2023 Tipo del documento: Article