Expression and role of the TRPC family in TGF-β1-induced calcium influx in podocytes.
- Author:
Hai-Ting HUANG
1
;
Xu LIN
2
;
Peng-Wei GUO
1
;
Jun PANG
1
;
Jing MA
1
;
Lin-Lin HE
1
;
Xin-Tong ZHENG
1
Author Information
1. Affiliated Hospital of Youjiang Medical University for Nationalities, Baise 533000, China.
2. Affiliated Hospital of Youjiang Medical University for Nationalities, Baise 533000, China. 00528@ymcn.edu.cn.
- Publication Type:Journal Article
- MeSH:
Animals;
TRPC6 Cation Channel/metabolism*;
Calcium/metabolism*;
TRPC Cation Channels/metabolism*;
Podocytes/metabolism*;
Transforming Growth Factor beta1/metabolism*;
RNA, Small Interfering/metabolism*;
RNA, Messenger/metabolism*;
Mammals/metabolism*
- From:
Acta Physiologica Sinica
2022;74(6):1005-1013
- CountryChina
- Language:Chinese
-
Abstract:
The TRPC family consists of multiple important cationic channels in mammals that participate in a variety of physiological and pathological processes. Our previous studies have shown that transforming growth factor-β1 (TGF-β1) increases the expression of TRPC6 in podocytes, but the roles of other members of the TRPC family in podocytes require further investigation. In this study, we investigated the effect of TGF-β1 on the expression of the TRPC family and the role of the TRPC family in the changes of the intracellular Ca2+ concentration ([Ca2+]i) in podocytes induced by TGF-β1. The model of podocyte injury was established by treatment with TGF-β1 in immortalized glomerular podocytes (MPC5) in vitro. qRT-PCR and Western blot were used to detect the effect of TGF-β1 on the mRNA and protein expression of each TRPC family member. After the expression of each TRPC family member was knocked down by a siRNA-based approach and blocked by SKF96365, respectively, free cytosolic Ca2+ was measured using the fluorescent Ca2+ indicator Fluo-3/AM, and the dynamic change of [Ca2+]i in podocytes was detected by a dynamic high-speed calcium imaging system. The results showed that TGF-β1 increased the protein expression of TRPC1/3/6 in podocytes, but had no effects on the protein expression of TRPC4. The protein expression levels of TRPC5/7 were only affected by 4 ng/mL and 8 ng/mL TGF-β1, respectively. TGF-β1 increased TRPC1/3/6 mRNA levels in podocytes, however had no effects on TRPC4/5/7 mRNA. TGF-β1 significantly increased [Ca2+]i in podocytes. Knockdown of TRPC1/4/5/7 in podocytes had no significant effect on the [Ca2+]i induced by TGF-β1, but TRPC3/6 knockdown significantly decreased the [Ca2+]i. There was no significant difference in the [Ca2+]i between the TRPC6 siRNA-treated group and SKF96365-treated group, but the [Ca2+]i of the TRPC3 siRNA-treated group was significantly higher than that of SKF96365-treated group. These results demonstrate that TGF-β1 increases the expression of the TRPC1/3/6 in podocytes. TGF-β1 increases [Ca2+]i in podocytes, which is dependent on the TRPC3/6 expression. Our results also suggest that the effect of TRPC6 on [Ca2+]i in podocytes may be greater than that of TRPC3.
