PTPσ inhibitors promote hematopoietic stem cell regeneration.
Yurun ZhangMartina RoosHeather HimburgChristina Marie TerminiMamle QuarmyneMichelle LiLiman ZhaoJenny KanTiancheng FangXiao YanKatherine PohlEmelyne DiersHyo Jin GimRobert DamoiseauxJulian P WhiteleggeWilliam McBrideMichael E JungJohn P ChutePublished in: Nature communications (2019)
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.
Keyphrases
- stem cells
- small molecule
- endothelial cells
- radiation induced
- protein protein
- induced pluripotent stem cells
- bone marrow
- wound healing
- pluripotent stem cells
- hematopoietic stem cell
- cell therapy
- radiation therapy
- binding protein
- type diabetes
- cell death
- young adults
- metabolic syndrome
- squamous cell carcinoma
- high fat diet induced
- mesenchymal stem cells
- locally advanced
- smoking cessation
- replacement therapy
- dna binding