| Literature DB >> 31451629 |
Fangfang Zhu1,2, Mingye Feng3, Rahul Sinha4,2, Matthew Philip Murphy4,2,5, Fujun Luo6, Kevin S Kao4,2, Krzysztof Szade4,2, Jun Seita4,2, Irving L Weissman1,7,8.
Abstract
GABRR1 is a rho subunit receptor of GABA, the major inhibitory neurotransmitter in the mammalian brain. While most investigations of its function focused on the nervous system, its regulatory role in hematopoiesis has not been reported. In this study, we found GABRR1 is mainly expressed on subsets of human and mouse hematopoietic stem cells (HSCs) and megakaryocyte progenitors (MkPs). GABRR1-negative (GR-) HSCs led to higher donor-derived hematopoietic chimerism than GABRR1-positive (GR+) HSCs. GR+ but not GR- HSCs and MkPs respond to GABA in patch clamp studies. Inhibition of GABRR1 via genetic knockout or antagonists inhibited MkP differentiation and reduced platelet numbers in blood. Overexpression of GABRR1 or treatment with agonists significantly promoted MkP generation and megakaryocyte colonies. Thus, this study identifies a link between the neural and hematopoietic systems and opens up the possibility of manipulating GABA signaling for platelet-required clinical applications.Entities:
Keywords: GABA; GABRR1; hematopoietic stem cell; megakaryocyte progenitors
Year: 2019 PMID: 31451629 PMCID: PMC6744911 DOI: 10.1073/pnas.1906251116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205