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PTPσ inhibitors promote hematopoietic stem cell regeneration

Authors :
Michelle Li
Liman Zhao
Heather A. Himburg
Tiancheng Fang
Yurun Zhang
Katherine Pohl
Martina Roos
Christina M. Termini
William H. McBride
Mamle Quarmyne
Robert Damoiseaux
Hyo Jin Gim
Michael E. Jung
Xiao Yan
John P. Chute
Julian P. Whitelegge
Emelyne Diers
Jenny Kan
Source :
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019), Nature Communications, Nature communications, vol 10, iss 1
Publication Year :
2019
Publisher :
Nature Portfolio, 2019.

Abstract

Receptor type protein tyrosine phosphatase-sigma (PTPσ) is primarily expressed by adult neurons and regulates neural regeneration. We recently discovered that PTPσ is also expressed by hematopoietic stem cells (HSCs). Here, we describe small molecule inhibitors of PTPσ that promote HSC regeneration in vivo. Systemic administration of the PTPσ inhibitor, DJ001, or its analog, to irradiated mice promotes HSC regeneration, accelerates hematologic recovery, and improves survival. Similarly, DJ001 administration accelerates hematologic recovery in mice treated with 5-fluorouracil chemotherapy. DJ001 displays high specificity for PTPσ and antagonizes PTPσ via unique non-competitive, allosteric binding. Mechanistically, DJ001 suppresses radiation-induced HSC apoptosis via activation of the RhoGTPase, RAC1, and induction of BCL-XL. Furthermore, treatment of irradiated human HSCs with DJ001 promotes the regeneration of human HSCs capable of multilineage in vivo repopulation. These studies demonstrate the therapeutic potential of selective, small-molecule PTPσ inhibitors for human hematopoietic regeneration.<br />Protein tyrosine phosphatase sigma (PTPσ) deficient haematopoietic stem cells (HSCs) demonstrate increased engraftment following transplantation. Here the authors identify a small molecule inhibitor of PTPσ that promotes murine and human haematopoietic stem cell regeneration via induction of the RAC pathway and BCL-XL.

Details

Language :
English
ISSN :
20411723
Volume :
10
Issue :
1
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....75ce2ccfb97329a8c01e40b8d756036f