IF1 restrains excessive elevation of the mitochondrial membrane potential and safeguards the epithelial state of human iPSCs
- 1University of the Ryukyus
Abstract
Human pluripotent stem cells (hPSCs) rely on glycolysis and exhibit low mitochondrial respiration, conditions under which F1Fo ATP synthase tends to run in reverse, hydrolyzing ATP. ATP synthase inhibitory factor subunit 1 (IF1) inhibits F1Fo-mediated ATP hydrolysis, but its significance in glycolytic hPSCs remains unclear. Here, we show that stable IF1 knockdown (IF1-KD) in human induced pluripotent stem cells (hiPSCs) enhanced mitochondrial ATP hydrolysis and elevated the mitochondrial membrane potential ({Delta}{Psi}m). Markers of the undifferentiated state were largely maintained, whereas IF1-KD cells exhibited reduced epithelial characteristics and a partial epithelial-mesenchymal transition (EMT)-like state. IF1-KD cells also showed enhanced store-operated Ca2 entry (SOCE) and increased nuclear NFATc3. Pharmacological reduction of {Delta}{Psi}m attenuated SOCE, whereas NFATc3 overexpression reproduced key features of the EMT-like expression pattern. Endogenous IF1 therefore acts as a constitutive restraint on reverse-mode F1Fo activity, limiting excessive {Delta}{Psi}m and downstream SOCE-NFATc3 signaling and safeguarding the epithelial state of hPSCs.
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BibTeX
@misc{kinjo2026restrains,
title = {{IF1 restrains excessive elevation of the mitochondrial membrane potential and safeguards the epithelial state of human iPSCs}},
author = {K. Kinjo and G. Takamatsu and K. Toyama and C. Takayama and Y. Akamine and R. Kuniyoshi and N. Otsuka and Y. Manome and H. J. Okano and C. Katagiri and M. Takatori and M. Matsushita},
howpublished = {bioRxiv},
year = {2026},
month = jun,
doi = {10.64898/2026.06.16.732339},
url = {https://www.biorxiv.org/content/10.64898/2026.06.16.732339v2},
note = {CC BY},
}
RIS
TY - UNPB
TI - IF1 restrains excessive elevation of the mitochondrial membrane potential and safeguards the epithelial state of human iPSCs
AU - K. Kinjo
AU - G. Takamatsu
AU - K. Toyama
AU - C. Takayama
AU - Y. Akamine
AU - R. Kuniyoshi
AU - N. Otsuka
AU - Y. Manome
AU - H. J. Okano
AU - C. Katagiri
AU - M. Takatori
AU - M. Matsushita
PY - 2026
DA - 2026/06/16
PB - bioRxiv
DO - 10.64898/2026.06.16.732339
UR - https://www.biorxiv.org/content/10.64898/2026.06.16.732339v2
AB - Human pluripotent stem cells (hPSCs) rely on glycolysis and exhibit low mitochondrial respiration, conditions under which F1Fo ATP synthase tends to run in reverse, hydrolyzing ATP. ATP synthase inhibitory factor subunit 1 (IF1) inhibits F1Fo-mediated ATP hydrolysis, but its significance in glycolytic hPSCs remains unclear. Here, we show that stable IF1 knockdown (IF1-KD) in human induced pluripotent stem cells (hiPSCs) enhanced mitochondrial ATP hydrolysis and elevated the mitochondrial membrane potential ({Delta}{Psi}m). Markers of the undifferentiated state were largely maintained, whereas IF1-KD cells exhibited reduced epithelial characteristics and a partial epithelial-mesenchymal transition (EMT)-like state. IF1-KD cells also showed enhanced store-operated Ca2 entry (SOCE) and increased nuclear NFATc3. Pharmacological reduction of {Delta}{Psi}m attenuated SOCE, whereas NFATc3 overexpression reproduced key features of the EMT-like expression pattern. Endogenous IF1 therefore acts as a constitutive restraint on reverse-mode F1Fo activity, limiting excessive {Delta}{Psi}m and downstream SOCE-NFATc3 signaling and safeguarding the epithelial state of hPSCs.
ER -