A human iPSC model with LATS1/2 knockdown (MUSIi012-A-9) for investigating Hippo signaling in stem cell

This study reports the generation and comprehensive characterization of the LATS1/2 knockdown (KD) induced pluripotent stem cell (iPSC) line, MUSIi012-A-9. Created via CRISPR/Cas9-mediated modification of the LATS2 gene in a parental LATS1-KD line, this resource serves as a crucial human model to investigate the roles of LATS1/2 kinases, key regulators of the Hippo signaling pathway. Comprehensive validation confirmed normal iPSC morphology, pluripotency marker expression (OCT3/4, NANOG, SOX2), genetic stability (46,XX karyotype), and robust multilineage differentiation potential. This well-characterized iPSC line is a vital tool for advancing research into Hippo pathway regulation, lineage specification, and cell fate determination in development and disease.

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Publication Details

Journal
Stem Cell Research
Published
2026-06-29
DOI
https://doi.org/10.1016/j.scr.2026.104052
Primary Topic
Hippo pathway signaling and YAP/TAZ
Type
article
Field-Weighted Citation Impact
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article

A human iPSC model with LATS1/2 knockdown (MUSIi012-A-9) for investigating Hippo signaling in stem cell

Chuti Laowtammathron, Phatchanat Klaihmon, Nittaya Jiamvoraphong, Surapol Issaragrisil et al.
Stem Cell Research
Hippo pathway signaling and YAP/TAZ
article

A human iPSC model with LATS1/2 knockdown (MUSIi012-A-9) for investigating Hippo signaling in stem cell

Chuti Laowtammathron, Phatchanat Klaihmon, Nittaya Jiamvoraphong, Surapol Issaragrisil, Chanchao Lorthongpanich, Pimonwan Srisook, Siriluk Kumsui
article en

Abstract

This study reports the generation and comprehensive characterization of the LATS1/2 knockdown (KD) induced pluripotent stem cell (iPSC) line, MUSIi012-A-9. Created via CRISPR/Cas9-mediated modification of the LATS2 gene in a parental LATS1-KD line, this resource serves as a crucial human model to investigate the roles of LATS1/2 kinases, key regulators of the Hippo signaling pathway. Comprehensive validation confirmed normal iPSC morphology, pluripotency marker expression (OCT3/4, NANOG, SOX2), genetic stability (46,XX karyotype), and robust multilineage differentiation potential. This well-characterized iPSC line is a vital tool for advancing research into Hippo pathway regulation, lineage specification, and cell fate determination in development and disease.

Stem Cell ResearchVol. 95
Agency for Science, Technology and Research (SG), Siriraj Hospital (TH), Mahidol University (TH), Institute of Molecular and Cell Biology (SG)
Openalex Percentile: Top 10%
Hippo pathway signaling and YAP/TAZ
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A human iPSC model with LATS1/2 knockdown (MUSIi012-A-9) for investigating Hippo signaling in stem cell — Chuti Laowtammathron, Phatchanat Klaihmon, et al. · Stem Cell Research (2026) | TGRS Research Map | TGRS