HDAC6 deacetylates IDH1 to promote the homeostasis of hematopoietic stem and progenitor cells

Author:

Yang Jia1ORCID,Liu Yang1,Yin Hanxiao1ORCID,Xie Songbo2ORCID,Zhang Linlin1ORCID,Dong Xifeng3,Ni Hua1,Bu Weiwen1ORCID,Ma Hongbo1,Liu Peng4,Zhu Haiyan4,Guo Rongxia4,Sun Lei2,Wu Yue2,Qin Juan1ORCID,Sun Baofa1ORCID,Li Dengwen1,Luo Hongbo R5ORCID,Liu Min6ORCID,Xuan Chenghao7ORCID,Zhou Jun12ORCID

Affiliation:

1. State Key Laboratory of Medicinal Chemical Biology, Haihe Laboratory of Cell Ecosystem, Tianjin Key Laboratory of Protein Science, College of Life Sciences Nankai University Tianjin China

2. Center for Cell Structure and Function, College of Life Sciences, Shandong Provincial Key Laboratory of Animal Resistance Biology, Collaborative Innovation Center of Cell Biology in Universities of Shandong Shandong Normal University Jinan China

3. Department of Hematology Tianjin Medical University General Hospital Tianjin China

4. State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Tianjin China

5. Department of Pathology, Department of Laboratory Medicine, Harvard Medical School Children's Hospital Boston, Dana‐Farber/Harvard Cancer Center Boston MA USA

6. Laboratory of Tissue Homeostasis Haihe Laboratory of Cell Ecosystem Tianjin China

7. The Province and Ministry Co‐sponsored Collaborative Innovation Center for Medical Epigenetics, Key Laboratory of Immune Microenvironment and Disease of the Ministry of Education, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences Tianjin Medical University Tianjin China

Abstract

AbstractHematopoietic stem and progenitor cells (HSPCs) are cells mainly present in the bone marrow and capable of forming mature blood cells. However, the epigenetic mechanisms governing the homeostasis of HSPCs remain elusive. Here, we demonstrate an important role for histone deacetylase 6 (HDAC6) in regulating this process. Our data show that the percentage of HSPCs in Hdac6 knockout mice is lower than in wild‐type mice due to decreased HSPC proliferation. HDAC6 interacts with isocitrate dehydrogenase 1 (IDH1) and deacetylates IDH1 at lysine 233. The deacetylation of IDH1 inhibits its catalytic activity and thereby decreases the 5‐hydroxymethylcytosine level of ten‐eleven translocation 2 (TET2) target genes, changing gene expression patterns to promote the proliferation of HSPCs. These findings uncover a role for HDAC6 and IDH1 in regulating the homeostasis of HSPCs and may have implications for the treatment of hematological diseases.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

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