TY - JOUR
T1 - Stage-specific gene expression in erythroid progenitor cells (CFU-E)
AU - Mishina, Yuji
AU - Matsui, Yasuhisa
AU - Obinata, Masuo
PY - 1988/2
Y1 - 1988/2
N2 - In erythropoietic differentiation, mature red blood cells are generated from specific progenitor cells through the action of specific growth regulatory molecules. To know the mechanism of differentiation, it is important to examine the control of gene expression in these progenitor cells in combination with growth regulatory molecules. We have cloned two genes expressing at a maximal level in the CFU-E (colony forming unit-erythroid), one of the erythroid progenitor cells from novel murine erythroleukemia (MEL) cell line (TSA8) which can be induced to CFU-E in vitro. The expression of these genes is well correlated with the appearance of CFU-E during induction of TSA8 cells, and is higher in the CFU-E-cells enriched from mouse fetal livers than in the more differentiated erythroid cells. Combining these with our previous results, it is suggested that in the erythropoiesis the progenitor cells have distinct patterns of gene expression. This expression is replaced through each progenitor cell rather than by the continuous increase in the expression of a set of genes specific to the mature erythroid cell following the commitment process.
AB - In erythropoietic differentiation, mature red blood cells are generated from specific progenitor cells through the action of specific growth regulatory molecules. To know the mechanism of differentiation, it is important to examine the control of gene expression in these progenitor cells in combination with growth regulatory molecules. We have cloned two genes expressing at a maximal level in the CFU-E (colony forming unit-erythroid), one of the erythroid progenitor cells from novel murine erythroleukemia (MEL) cell line (TSA8) which can be induced to CFU-E in vitro. The expression of these genes is well correlated with the appearance of CFU-E during induction of TSA8 cells, and is higher in the CFU-E-cells enriched from mouse fetal livers than in the more differentiated erythroid cells. Combining these with our previous results, it is suggested that in the erythropoiesis the progenitor cells have distinct patterns of gene expression. This expression is replaced through each progenitor cell rather than by the continuous increase in the expression of a set of genes specific to the mature erythroid cell following the commitment process.
KW - CFU-E (colony forming unit-erythroid)
KW - Induction-specific cDNA clone
KW - Murine erythroleukemia cell
KW - Sequential gene expression
UR - http://www.scopus.com/inward/record.url?scp=0023838002&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0023838002&partnerID=8YFLogxK
U2 - 10.1016/0045-6039(88)90017-6
DO - 10.1016/0045-6039(88)90017-6
M3 - Article
C2 - 3162713
AN - SCOPUS:0023838002
SN - 0045-6039
VL - 22
SP - 259
EP - 265
JO - Cell Differentiation
JF - Cell Differentiation
IS - 3
ER -