Elevated mitochondrial protein import in acute myeloid leukemia increases reliance on mitochondrial protease LONP1

Most mitochondrial proteins are nuclear encoded, translated in the cytosol, and imported into the mitochondria. Through gene expression analysis and functional assays, we demonstrated that mitochondrial protein import is increased in acute myeloid leukemia (AML) cells compared to normal hematopoietic cells. Increased mitochondrial protein import was positively correlated with increased mitochondrial unfolded protein response (UPRmt), a stress activated pathway of mitochondrial proteases and chaperones that maintains protein solubility and prevents the formation of toxic aggregates. The UPRmt protease LONP1 (Lon Peptidase 1) was upregulated in AML and positively correlated with increased mitochondrial protein import and UPRmt. Genetically or chemically inhibiting the LONP1 ATPase domain induced mitochondrial protein aggregation and selectively killed AML cells with high LONP1 expression while sparing AML cells with low LONP1 expression and normal hematopoietic cells in vitro and in vivo. Thus, we uncovered a critical role of the UPRmt protease LONP1 in buffering stress from mitochondrial protein import in AML.

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Publication Details

Journal
Journal of Clinical Investigation
Published
2026-06-16
DOI
https://doi.org/10.1172/jci196687
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
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article

Elevated mitochondrial protein import in acute myeloid leukemia increases reliance on mitochondrial protease LONP1

Chaitra Sarathy, Véronique Voisin, Shahbaz Khan, Matthew Tcheng et al.
Journal of Clinical Investigation
Mitochondrial Function and Pathology
article

Elevated mitochondrial protein import in acute myeloid leukemia increases reliance on mitochondrial protease LONP1

Chaitra Sarathy, Véronique Voisin, Shahbaz Khan, Matthew Tcheng, Yulia Jitkova, Rose Hurren, Lan-Xin Zhang, Geethu Emily Thomas, Ross S. Mancini, Thomas Kislinger, Edward Ayoub, Nathan Duong, Po Yee Mak, Siavash Vahidi, Marcela Gronda, Dakai Ling, Andrea Arruda, Yongran Yan, Ali Chegini, Feng Yue, Bing Z. Carter, Michael Andreeff, S M Kornblau, Zaynab Mamai, Brady Stock, Anastasija A. Piric, Aaron D. Schimmer, Mark D. Minden, Stefan Quinn W. Currie, Mark Reed
article en

Abstract

Most mitochondrial proteins are nuclear encoded, translated in the cytosol, and imported into the mitochondria. Through gene expression analysis and functional assays, we demonstrated that mitochondrial protein import is increased in acute myeloid leukemia (AML) cells compared to normal hematopoietic cells. Increased mitochondrial protein import was positively correlated with increased mitochondrial unfolded protein response (UPRmt), a stress activated pathway of mitochondrial proteases and chaperones that maintains protein solubility and prevents the formation of toxic aggregates. The UPRmt protease LONP1 (Lon Peptidase 1) was upregulated in AML and positively correlated with increased mitochondrial protein import and UPRmt. Genetically or chemically inhibiting the LONP1 ATPase domain induced mitochondrial protein aggregation and selectively killed AML cells with high LONP1 expression while sparing AML cells with low LONP1 expression and normal hematopoietic cells in vitro and in vivo. Thus, we uncovered a critical role of the UPRmt protease LONP1 in buffering stress from mitochondrial protein import in AML.

Journal of Clinical Investigation
University Health Network (CA), The University of Texas MD Anderson Cancer Center (US), Princess Margaret Cancer Centre (CA), Ontario Brain Institute (CA), University of Guelph (CA)
Openalex Percentile: Top 12%
Mitochondrial Function and Pathology
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