Stable bioreactor control reveals acidic pH–driven metabolic reprogramming and mitochondrial dysfunction in human lymphoblastoid cells

levels by NMN or PARP1 inhibition reverses heteroplasmic enrichment of mutant mitochondrial DNA. These findings underscore the role of pH homeostasis in coordinating metabolism, redox balance, and immune signaling, and identify NAD⁺ metabolism as a mechanistic link between acidic microenvironments, mitochondrial genome instability, and immune-metabolic remodeling.

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Publication Details

Journal
Communications Biology
Published
2026-04-15
DOI
https://doi.org/10.1038/s42003-026-10013-5
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.00
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article

Stable bioreactor control reveals acidic pH–driven metabolic reprogramming and mitochondrial dysfunction in human lymphoblastoid cells

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Communications Biology
Mitochondrial Function and Pathology
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Stable bioreactor control reveals acidic pH–driven metabolic reprogramming and mitochondrial dysfunction in human lymphoblastoid cells

Samhan Alsolami, Mengge Wang, Shannon G. Klein, Nadia Steiner, Yiqing Jin, Kacper Szczepski, Pierre Julius Magistretti, Juan Carlos Izpisúa Belmonte, Chongwei Bi, Łukasz Jaremko, Carlos Manuel Duarte, Mo Li, Baolei Yuan, Siyi Fu, Yingzi Zhang
article en

Abstract

levels by NMN or PARP1 inhibition reverses heteroplasmic enrichment of mutant mitochondrial DNA. These findings underscore the role of pH homeostasis in coordinating metabolism, redox balance, and immune signaling, and identify NAD⁺ metabolism as a mechanistic link between acidic microenvironments, mitochondrial genome instability, and immune-metabolic remodeling.

Communications Biology
Altos Labs, The University of Texas Medical Branch at Galveston (US), King Abdullah University of Science and Technology (SA)
Life in Land
Openalex Percentile: Top 19%
Mitochondrial Function and Pathology
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