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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 |
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container_issue | 6 |
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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 |
format | article |
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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.</description><identifier>ISSN: 1749-0774</identifier><identifier>ISSN: 0914-7470</identifier><identifier>EISSN: 1749-0774</identifier><identifier>DOI: 10.1007/s13577-022-00777-3</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>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</subject><ispartof>Human cell : official journal of Human Cell Research Society, 2022-11, Vol.35 (6), p.1722-1735</ispartof><rights>The Author(s) under exclusive licence to Japan Human Cell Society 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-40046eca9781f517c908a7a0db986d63088d3bbfa43e46a8a2671ee84c6f02dd3</citedby><cites>FETCH-LOGICAL-c376t-40046eca9781f517c908a7a0db986d63088d3bbfa43e46a8a2671ee84c6f02dd3</cites><orcidid>0000-0002-2884-0736</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Shen, Jie</creatorcontrib><creatorcontrib>Wu, Xiushan</creatorcontrib><creatorcontrib>Zhu, Ping</creatorcontrib><creatorcontrib>Zhuang, Jian</creatorcontrib><creatorcontrib>Qin, Bin</creatorcontrib><creatorcontrib>Sun, Fang</creatorcontrib><creatorcontrib>Yuan, Wuzhou</creatorcontrib><creatorcontrib>Fan, Xiongwei</creatorcontrib><creatorcontrib>Jiang, Zhigang</creatorcontrib><creatorcontrib>Li, Fang</creatorcontrib><creatorcontrib>Li, Yongqing</creatorcontrib><creatorcontrib>Wang, Yuequn</creatorcontrib><creatorcontrib>Zhao, Mingyi</creatorcontrib><title>Overexpression of PYGO1 promotes early cardiac lineage development in human umbilical cord mesenchymal stromal/stem cells by activating the Wnt/β-catenin pathway</title><title>Human cell : official journal of Human Cell Research Society</title><addtitle>Human Cell</addtitle><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.</description><subject>Biomedical and Life Sciences</subject><subject>Cardiovascular diseases</subject><subject>Cell Biology</subject><subject>Embryogenesis</subject><subject>Flow cytometry</subject><subject>Gene expression</subject><subject>Gynecology</subject><subject>Heart</subject><subject>Immunofluorescence</subject><subject>Islet-1 protein</subject><subject>Life Sciences</subject><subject>Mesenchyme</subject><subject>Nkx2.5 protein</subject><subject>Oncology</subject><subject>Proteins</subject><subject>Reproductive Medicine</subject><subject>Research Article</subject><subject>Stem Cells</subject><subject>Surgery</subject><subject>Umbilical cord</subject><subject>Wnt protein</subject><subject>β-Catenin</subject><issn>1749-0774</issn><issn>0914-7470</issn><issn>1749-0774</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kU2O1DAQhSMEEsPABVhZYsMmtB27bWeJRjCMNFKzACFWVsWpdHuU2MF2GnIdjsBB5ky4aSQQC1b1o-89VelV1XNGXzFK1SYxvlWqpk1Tl7F0_EF1wZRo6zKJh3_1j6snKd1RKrZCNhfV990RI36bI6bkgidhIO8_X-8YmWOYQsZEEOK4Eguxd2DJ6DzCHkmPRxzDPKHPxHlyWCbwZJk6NzoLI7Eh9mTChN4e1qksUi5-MG5SxolYHMdEupWAze4I2fk9yQckn3ze3P-oLWT0xXSGfPgK69Pq0QBjwme_62X18e2bD1fv6tvd9c3V69vaciVzLcpPEi20SrNhy5RtqQYFtO9aLXvJqdY977oBBEchQUMjFUPUwsqBNn3PL6uXZ9_y-pcFUzaTS6dTwWNYkmkUa7RoBRUFffEPeheW6Mt1J0pLqZVsC9WcKRtDShEHM0c3QVwNo-YUmznHZkps5ldshhcRP4tSgf0e4x_r_6h-AgYAnrg</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>Shen, Jie</creator><creator>Wu, Xiushan</creator><creator>Zhu, Ping</creator><creator>Zhuang, Jian</creator><creator>Qin, Bin</creator><creator>Sun, Fang</creator><creator>Yuan, Wuzhou</creator><creator>Fan, Xiongwei</creator><creator>Jiang, Zhigang</creator><creator>Li, Fang</creator><creator>Li, Yongqing</creator><creator>Wang, Yuequn</creator><creator>Zhao, Mingyi</creator><general>Springer Nature Singapore</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2884-0736</orcidid></search><sort><creationdate>20221101</creationdate><title>Overexpression of PYGO1 promotes early cardiac lineage development in human umbilical cord mesenchymal stromal/stem cells by activating the Wnt/β-catenin pathway</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-40046eca9781f517c908a7a0db986d63088d3bbfa43e46a8a2671ee84c6f02dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biomedical and Life Sciences</topic><topic>Cardiovascular diseases</topic><topic>Cell Biology</topic><topic>Embryogenesis</topic><topic>Flow cytometry</topic><topic>Gene expression</topic><topic>Gynecology</topic><topic>Heart</topic><topic>Immunofluorescence</topic><topic>Islet-1 protein</topic><topic>Life Sciences</topic><topic>Mesenchyme</topic><topic>Nkx2.5 protein</topic><topic>Oncology</topic><topic>Proteins</topic><topic>Reproductive Medicine</topic><topic>Research Article</topic><topic>Stem Cells</topic><topic>Surgery</topic><topic>Umbilical cord</topic><topic>Wnt protein</topic><topic>β-Catenin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Jie</creatorcontrib><creatorcontrib>Wu, Xiushan</creatorcontrib><creatorcontrib>Zhu, Ping</creatorcontrib><creatorcontrib>Zhuang, Jian</creatorcontrib><creatorcontrib>Qin, Bin</creatorcontrib><creatorcontrib>Sun, Fang</creatorcontrib><creatorcontrib>Yuan, Wuzhou</creatorcontrib><creatorcontrib>Fan, Xiongwei</creatorcontrib><creatorcontrib>Jiang, Zhigang</creatorcontrib><creatorcontrib>Li, Fang</creatorcontrib><creatorcontrib>Li, Yongqing</creatorcontrib><creatorcontrib>Wang, Yuequn</creatorcontrib><creatorcontrib>Zhao, Mingyi</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Human cell : official journal of Human Cell Research Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Jie</au><au>Wu, Xiushan</au><au>Zhu, Ping</au><au>Zhuang, Jian</au><au>Qin, Bin</au><au>Sun, Fang</au><au>Yuan, Wuzhou</au><au>Fan, Xiongwei</au><au>Jiang, Zhigang</au><au>Li, Fang</au><au>Li, Yongqing</au><au>Wang, Yuequn</au><au>Zhao, Mingyi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of PYGO1 promotes early cardiac lineage development in human umbilical cord mesenchymal stromal/stem cells by activating the Wnt/β-catenin pathway</atitle><jtitle>Human cell : official journal of Human Cell Research Society</jtitle><stitle>Human Cell</stitle><date>2022-11-01</date><risdate>2022</risdate><volume>35</volume><issue>6</issue><spage>1722</spage><epage>1735</epage><pages>1722-1735</pages><issn>1749-0774</issn><issn>0914-7470</issn><eissn>1749-0774</eissn><abstract>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.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><doi>10.1007/s13577-022-00777-3</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-2884-0736</orcidid></addata></record> |
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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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