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RA signaling pathway combined with Wnt signaling pathway regulates human-induced pluripotent stem cells (hiPSCs) differentiation to sinus node-like cells.

Authors :
Yin, Lin
Wang, Feng-yuan
Zhang, Wei
Wang, Xi
Tang, Yan-hong
Wang, Teng
Chen, Yu-ting
Huang, Cong-xin
Source :
Stem Cell Research & Therapy; 7/18/2022, Vol. 13 Issue 1, p1-15, 15p
Publication Year :
2022

Abstract

Background: The source of SAN is debated among researchers. Many studies have shown that RA and Wnt signaling are involved in heart development. In this study, we investigated the role of retinoic acid (RA) and Wnt signaling in the induction of sinus node-like cells. Methods: The experimental samples were divided into four groups: control group (CHIR = 0), CHIR = 3, RA + CHIR = 0 andRA + CHIR = 3. After 20 days of differentiation, Western blot, RT-qPCR, immunofluorescence and flow cytometry were performed to identify sinus node-like cells. Finally, whole-cell patch clamp technique was used to record pacing funny current and action potential (AP) in four groups. Results: The best intervention method used in our experiment was RA = 0.25 µmol/L D5-D9 + CHIR = 3 µmol/L D5-D7. Results showed that CHIR can increase the expression of ISL-1 and TBX3, while RA mainly elevated Shox2. Immunofluorescence assay and flow cytometry further illustrated that combining RA with CHIR can induce sinus node-like cells (CTNT<superscript>+</superscript>Shox2<superscript>+</superscript>Nkx2.5<superscript>−</superscript>). Moreover, CHIR might reduce the frequency of cell beats, but in conjunction with RA could partly compensate for this side effect. Whole cell patch clamps were able to record funny current and the typical sinus node AP in the experimental group, which did not appear in the control group. Conclusions: Combining RA with Wnt signaling within a specific period can induce sinus node-like cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17576512
Volume :
13
Issue :
1
Database :
Complementary Index
Journal :
Stem Cell Research & Therapy
Publication Type :
Academic Journal
Accession number :
158036139
Full Text :
https://doi.org/10.1186/s13287-022-03006-8