TY - JOUR
T1 - Leucine-rich Repeat-containing G-protein-coupled receptor 5 marks short-term hematopoietic stem and progenitor cells during mouse embryonic development
AU - Liu, Donghua
AU - He, Xi C.
AU - Qian, Pengxu
AU - Barker, Nick
AU - Trainor, Paul A.
AU - Clevers, Hans
AU - Liu, Huiwen
AU - Li, Linheng
PY - 2014
Y1 - 2014
N2 - Lgr5 is a marker for proliferating stem cells in adult intestine, stomach, and hair follicle. However, Lgr5 is not expressed in adult hematopoietic stem and progenitor cells (HSPCs). Whether Lgr5 is expressed in the embryonic and fetal HSPCs that undergo rapid proliferation is unknown. Here we report the detection of Lgr5 expression in HSPCs in the aorta-gonad-mesonephros (AGM) and fetal liver.Wealso found that a portion of Lgr5+ cells expressed the Runx1 gene that is critical for the ontogeny of HSPCs. A small portion of Lgr5+ cells also expressed HSPC surface markers c-Kit and CD34 in AGM or CD41 in fetal liver. Furthermore, the majority of Lgr5+ cells expressed Ki67, indicating their proliferating state. Transplantation of fetal liver-derived Lgr5-GFP- cells (E12.5) demonstrated that Lgr5-GFP - cells were able to reconstitute myeloid and lymphoid lineages in adult recipients, but the engraftment was short-term (4-8 weeks) and 20-fold lower compared with the Lgr5-GFP- control. Our data show that Lgr5-expressing cells mark short-term hematopoietic stem and progenitor cells, consistent with the role of Lgr5 in supporting HSPCs rapid proliferation during embryonic and fetal development.
AB - Lgr5 is a marker for proliferating stem cells in adult intestine, stomach, and hair follicle. However, Lgr5 is not expressed in adult hematopoietic stem and progenitor cells (HSPCs). Whether Lgr5 is expressed in the embryonic and fetal HSPCs that undergo rapid proliferation is unknown. Here we report the detection of Lgr5 expression in HSPCs in the aorta-gonad-mesonephros (AGM) and fetal liver.Wealso found that a portion of Lgr5+ cells expressed the Runx1 gene that is critical for the ontogeny of HSPCs. A small portion of Lgr5+ cells also expressed HSPC surface markers c-Kit and CD34 in AGM or CD41 in fetal liver. Furthermore, the majority of Lgr5+ cells expressed Ki67, indicating their proliferating state. Transplantation of fetal liver-derived Lgr5-GFP- cells (E12.5) demonstrated that Lgr5-GFP - cells were able to reconstitute myeloid and lymphoid lineages in adult recipients, but the engraftment was short-term (4-8 weeks) and 20-fold lower compared with the Lgr5-GFP- control. Our data show that Lgr5-expressing cells mark short-term hematopoietic stem and progenitor cells, consistent with the role of Lgr5 in supporting HSPCs rapid proliferation during embryonic and fetal development.
UR - http://www.scopus.com/inward/record.url?scp=84906536746&partnerID=8YFLogxK
U2 - 10.1074/jbc.M114.568170
DO - 10.1074/jbc.M114.568170
M3 - Article
C2 - 24966324
AN - SCOPUS:84906536746
SN - 0021-9258
VL - 289
SP - 23809
EP - 23816
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 34
ER -