TY - JOUR
T1 - Production of PDGF-like growth factors by embryonal carcinoma cells and binding of PDGF to their endoderm-like differentiated cells
AU - Rizzino, Angie
AU - Bowen-Pope, Daniel F.
N1 - Funding Information:
We thank Linda Dorman for technical assistance and Heather Rizzino for editorial assistance. We also thank E. Raines and R. Ross for the generous gifts of purified PDGF and anti-PDGF antibodies. Part of this research (A.R.) was supported by, and performed at, the National Cancer Institute, Frederick, Md. and by grants (SO7 RR05391 and 22-271-732) from the University of Nebraska Medical Center and a grant (CA 36727) from the National Cancer Institute. This research was also supported (D.B.-P.) by NIH Grant HL 18645, plus grants from R. J. Reynolds, Inc. and the Life and Health Insurance Medical Research Fund.
PY - 1985/7
Y1 - 1985/7
N2 - In this report, we demonstrate that F9 and PC-13 embryonal carcinoma (EC) cells do not bind significant amounts of platelet-derived growth factor (PDGF), whereas the endoderm-like differentiated cells derived from EC cells do. The F9-differentiated cells exhibit approximately 8300 receptors per cell, with an apparent dissociation constant of 30 pM. Two endoderm-like cell lines, PSA-5E and PYS-2, also bind PDGF and exhibit approximately 4800 and 23,500 receptors per cell, respectively. The lack of PDGF binding by the parental EC cells is consistent with their release of a factor(s) that is closely related to PDGF. This factor(s) competes with PDGF for binding to membrane receptors and is recognized by antibodies raised against PDGF. However, this factor(s) does not appear to be antigenically identical to PDGF. We also show that production of this PDGF-like factor(s) is reduced more than 90% when F9 EC cells differentiate into cells that bind PDGF. Thus, our findings indicate that EC cells release a factor(s) that should be capable of binding to their differentiated cells. This raises the possibility that PDGF, or a closely related factor, can influence cell proliferation and/or cell behavior of early embryonic cells.
AB - In this report, we demonstrate that F9 and PC-13 embryonal carcinoma (EC) cells do not bind significant amounts of platelet-derived growth factor (PDGF), whereas the endoderm-like differentiated cells derived from EC cells do. The F9-differentiated cells exhibit approximately 8300 receptors per cell, with an apparent dissociation constant of 30 pM. Two endoderm-like cell lines, PSA-5E and PYS-2, also bind PDGF and exhibit approximately 4800 and 23,500 receptors per cell, respectively. The lack of PDGF binding by the parental EC cells is consistent with their release of a factor(s) that is closely related to PDGF. This factor(s) competes with PDGF for binding to membrane receptors and is recognized by antibodies raised against PDGF. However, this factor(s) does not appear to be antigenically identical to PDGF. We also show that production of this PDGF-like factor(s) is reduced more than 90% when F9 EC cells differentiate into cells that bind PDGF. Thus, our findings indicate that EC cells release a factor(s) that should be capable of binding to their differentiated cells. This raises the possibility that PDGF, or a closely related factor, can influence cell proliferation and/or cell behavior of early embryonic cells.
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U2 - 10.1016/0012-1606(85)90058-2
DO - 10.1016/0012-1606(85)90058-2
M3 - Article
C2 - 2989042
AN - SCOPUS:0021809229
SN - 0012-1606
VL - 110
SP - 15
EP - 22
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -