Menu
Currency
Research Publication

Mitochondrial retrograde signaling initiates HIF-1α/BNIP3/NIX-mediated mitophagy in Tibetan high-altitude adaptation.

Wei Yang, Y Sun, Dayan D et al.

41490888 PubMed ID
19 Authors
2026-01-06 Published
117 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WY
Wei Yang
YS
Y Sun
DD
Dayan D
WF
Wu Fei
FZ
F Zhang
SS
Shixuan S
CB
Cai Bowen
BM
B Ma
YY
Yanyun Y
ZH
Zheng Hongxiang
HS
H Shi
XX
Xiangguang X
LY
Li Yi
YL
Y Le
SS
Shiguan S
ZX
Zhou Xiang
XJ
X Jin
LL
Li L
WJ
Wang Jiucun
Chapter II

Abstract

Summary of the research findings

Genome-wide studies have identified the nuclear gene EPAS1 and the mitochondrial M9a haplogroup as pivotal contributors to hypoxia adaptation in Tibetans. However, the interaction between these two genetic components is not yet clear. In this study, we demonstrate that cells harboring the Tibetan-specific M9a haplogroup with downregulated EPAS1 (M9a+shEPAS1) exhibit enhanced cellular function under hypoxic conditions. These cells display improved mitochondrial function and proliferation, alongside reduced apoptosis and mtDNA-mediated inflammation, driven by the activation of HIF-1α-BNIP3/NIX-mediated mitophagy and an increase in reactive oxygen species (ROS) levels. Furthermore, treatment with N-acetylcysteine (NAC), PX-478, or Mdivi-1 significantly attenuated BNIP3/NIX-mediated mitophagy, leading to an aggravation of mtDNA-mediated inflammation and apoptosis in M9a+shEPAS1 cells during hypoxia. This study first reveals that ROS-driven HIF-1α-BNIP3/NIX-mediated mitophagy mitigates hypoxia-induced inflammation and apoptosis, contributing to the enhanced hypoxia adaptation observed in Tibetans. HIF-1α-BNIP3/NIX-mediated mitophagy may offer potential therapeutic targets for high-altitude illnesses by regulating cellular energy metabolism and inflammation.

Chapter III

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of ancestry and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

Summary

Key Findings

Ancestry Insights

Traits Analysis

Historical Context