Fig. 7.
Fig. 7. A possible model for coordinated development of HSCs and liver. / LTR HSCs with CD34+/c-Kit+ generated in AGM immediately migrate to the FL. Factors including OSM that are secreted from hematopoietic cells induce maturation of hepatic cells as a metabolic organ. The hepatic cells, in turn, stimulate expansion and maturation of AGM HSCs to FL HSCs with reduced proliferation potential. The fetal hepatic cells provide a hematopoietic microenvironment suitable for expansion of AGM HSCs but not of FL HSCs. Accordingly, HSCs migrate from the liver to bone marrow, the final destination of HSCs.

A possible model for coordinated development of HSCs and liver.

LTR HSCs with CD34+/c-Kit+ generated in AGM immediately migrate to the FL. Factors including OSM that are secreted from hematopoietic cells induce maturation of hepatic cells as a metabolic organ. The hepatic cells, in turn, stimulate expansion and maturation of AGM HSCs to FL HSCs with reduced proliferation potential. The fetal hepatic cells provide a hematopoietic microenvironment suitable for expansion of AGM HSCs but not of FL HSCs. Accordingly, HSCs migrate from the liver to bone marrow, the final destination of HSCs.

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