Pearson syndrome-like anemia induced by accumulation of mutant mtDNA and anemia with imbalanced white blood cell lineages induced by Drp1 deletion in a murine model-Reference-Cited by-同舟云学术

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Pearson syndrome-like anemia induced by accumulation of mutant mtDNA and anemia with imbalanced white blood cell lineages induced by Drp1 deletion in a murine model

Published:2022-11 Issue: Volume:185 Page:106467
ISSN:1043-6618
Container-title:Pharmacological Research
language:en
Short-container-title:Pharmacological Research

Author:

Ishikawa Kaori,Honma Yo,Yoshimi Ayami,Katada Shun,Ishihara Takaya,Ishihara Naotada,Nakada Kazuto

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Japan Science and Technology Agency

Bundesministerium für Bildung und Forschung

Core Research for Evolutional Science and Technology

Publisher

Elsevier BV

Subject

Pharmacology

Reference34 articles.

1. Connecting mitochondria, metabolism, and stem cell fate;Wanet;Stem Cells Dev.,2015

2. Specification of haematopoietic stem cell fate via modulation of mitochondrial activity;Vannini;Nat. Commun.,2016

3. The distinct metabolic profile of hematopoietic stem cells reflects their location in a hypoxic niche;Simsek;Cell Stem Cell,2010

4. TSC-mTOR maintains quiescence and function of hematopoietic stem cells by repressing mitochondrial biogenesis and reactive oxygen species;Chen;J. Exp. Med.,2008

5. Mito-protective autophagy is impaired in erythroid cells of aged mtDNA-mutator mice;Li-Harms;Blood,2015

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