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Overexpression of PYGO1 promotes early cardiac lineage development in human umbilical cord mesenchymal stromal/stem cells by activating the Wnt/β-catenin pathway

Cardiovascular disease still has the highest mortality. Gene‐modified mesenchymal stromal/stem cells could be a promising therapy. Pygo plays an important role in embryonic development and regulates life activities with a variety of regulatory mechanisms. Therefore, this study aimed to investigate w...

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Published in:Human cell : official journal of Human Cell Research Society 2022-11, Vol.35 (6), p.1722-1735
Main Authors: Shen, Jie, Wu, Xiushan, Zhu, Ping, Zhuang, Jian, Qin, Bin, Sun, Fang, Yuan, Wuzhou, Fan, Xiongwei, Jiang, Zhigang, Li, Fang, Li, Yongqing, Wang, Yuequn, Zhao, Mingyi
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container_title Human cell : official journal of Human Cell Research Society
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creator Shen, Jie
Wu, Xiushan
Zhu, Ping
Zhuang, Jian
Qin, Bin
Sun, Fang
Yuan, Wuzhou
Fan, Xiongwei
Jiang, Zhigang
Li, Fang
Li, Yongqing
Wang, Yuequn
Zhao, Mingyi
description Cardiovascular disease still has the highest mortality. Gene‐modified mesenchymal stromal/stem cells could be a promising therapy. Pygo plays an important role in embryonic development and regulates life activities with a variety of regulatory mechanisms. Therefore, this study aimed to investigate whether the overexpression of the PYGO1 gene can promote the differentiation of human umbilical cord-derived mesenchymal stromal/stem cells (HUC-MSCs) into early cardiac lineage cells and to preliminary explore the relevant mechanisms. In this study, HUC-MSCs were isolated by the explant method and were identified by flow cytometry and differentiation assay, followed by transfected with lentivirus carrying the PYGO1 plasmid. In PYGO1 group (cells were incubated with lentiviral- PYGO1 ), the mRNA expressions of cardiac differentiation-specific markers ( MESP1 , NKX2.5 , GATA4 , MEF2C , ISL1 , TBX5, TNNT2 , ACTC1 , and MYH6 genes) and the protein expressions of NKX2.5 and cTnT were significantly up-regulated compared with the NC group (cells were incubated with lentiviral-empty vector). In addition, the proportion of NKX2.5, GATA4, and cTnT immunofluorescence-positive cells increased with the inducement time. Overexpression of PYGO1 statistically significantly increased the relative luciferase expression level of Topflash plasmid, the protein expression level of β-catenin and the mRNA expression level of CYCLIND1. Compared with the control group, decreased protein levels of NKX2.5 and cTnT were detected in PYGO1 group after application of XAV-939, the specific inhibitor of the canonical Wnt/β-catenin pathway. Our study suggests that overexpression of PYGO1 significantly promotes the differentiation of HUC-MSCs into early cardiac lineage cells, which is regulated by the canonical Wnt/β-catenin signaling.
doi_str_mv 10.1007/s13577-022-00777-3
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Gene‐modified mesenchymal stromal/stem cells could be a promising therapy. Pygo plays an important role in embryonic development and regulates life activities with a variety of regulatory mechanisms. Therefore, this study aimed to investigate whether the overexpression of the PYGO1 gene can promote the differentiation of human umbilical cord-derived mesenchymal stromal/stem cells (HUC-MSCs) into early cardiac lineage cells and to preliminary explore the relevant mechanisms. In this study, HUC-MSCs were isolated by the explant method and were identified by flow cytometry and differentiation assay, followed by transfected with lentivirus carrying the PYGO1 plasmid. 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subjects Biomedical and Life Sciences
Cardiovascular diseases
Cell Biology
Embryogenesis
Flow cytometry
Gene expression
Gynecology
Heart
Immunofluorescence
Islet-1 protein
Life Sciences
Mesenchyme
Nkx2.5 protein
Oncology
Proteins
Reproductive Medicine
Research Article
Stem Cells
Surgery
Umbilical cord
Wnt protein
β-Catenin
title Overexpression of PYGO1 promotes early cardiac lineage development in human umbilical cord mesenchymal stromal/stem cells by activating the Wnt/β-catenin pathway
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