Premium
Megakaryocytes promote hepatoepithelial liver cell development in E11.5 mouse embryos by cell‐to‐cell contact and by vascular endothelial growth factor A signaling
Author(s) -
Serrano Natalia,
Cortegano Isabel,
Ruiz Carolina,
Alía Mario,
de Andrés Belén,
Rejas María Teresa,
Marcos Miguel A.R.,
Gaspar María Luisa
Publication year - 2012
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.25853
Subject(s) - biology , microbiology and biotechnology , progenitor cell , hepatocyte growth factor , megakaryocyte , immunology , thrombopoietin , endothelial stem cell , haematopoiesis , stem cell , in vitro , receptor , biochemistry
In the mouse embryo, hematopoietic progenitor cells migrate to the fetal liver (FL) between gestational days (E) 9.5 and 10.5, where they rapidly expand to form the main fetal reservoir of hematopoietic cells. The embryonic megakaryocyte progenitors (MKPs) in the E11.5 FL were identified as CD49f H CD41 H (and c‐Kit D KDR + CD42 + CD9 ++ CD31 + ) cells, expressing several hepato‐specific proteins. Unlike adult bone marrow megakaryocytes (MKs), embryonic MKPs were CD45 − and represent an abundant population in the FL. The CD49f H CD41 H MKPs purified by cytometry differentiated in vitro to produce proplatelets, independent of thrombopoietin stimulation, and they responded to stimulation with adenosine diphosphate, thrombin, and the PAR4 thrombin receptor‐activating peptide. Moreover, after removing CD49f H CD41 H MKPs from purified E11.5 FL hepatoepithelial‐enriched cell preparations (c‐Kit D CD45 − Ter119 − ), the remaining CD49f D cells neither differentiated nor survived in vitro . Indeed, direct cell‐to‐cell contact between the CD49f H CD41 H and CD49f D populations was required to promote the hepatocyte differentiation of CD49f D cells. The addition of vascular endothelial growth factor A (VEGF‐A) and medium conditioned by E11.5 CD49f H CD41 H MKPs produced a partial effect on CD49f D cells, inducing the formation of hepatoepithelial layers. This effect was abolished by anti‐VEGF‐A antibodies. Together, these findings strongly suggest that CD49f H CD41 H MKPs are fundamental to promote FL development, as proposed in adult liver regeneration. Conclusion: The cells of the MK lineage present in the developing mouse embryo liver promote the growth of hepatoepithelial cells in vitro through VEGF‐A signaling and may play a role in liver development in vivo . (H EPATOLOGY 2012;56:1934–1945)