TY - JOUR
T1 - Role of growth factors in the contraction and maintenance of collagen lattices made with arterial smooth muscle cells
AU - Chen, Jan‐Kan ‐K
AU - Haimes, Howard B.
AU - Weinberg, Crispin B.
PY - 1991/1
Y1 - 1991/1
N2 - The contraction of collagen lattices made with arterial smooth muscle cells was studied in medium MCDB 107 without serum or supplemented with 1% fetal bovine serum, plus insulin, transferrin, and low‐density lipoprotein. Under these conditions, smooth muscle cell mitogens including HBGF‐1 (aFGF), PDGF, and EGF stimulated contraction. Stimulation by HBGF‐1 was more profound than with other factors tested. HBGF‐1 stimulation of lattice contraction was blocked by protein synthesis inhibitors, but not by inhibitors of DNA synthesis. Histological observations indicated that HBGF‐1 also enhanced the maintenance of healthy cells in the lattice. Taken together, these observations suggest that HBGF‐1 stimulates lattice contraction, not by a mitogenic effect, but by stimulating synthesis of specific cellular proteins. Since the greatest effects of HBGF‐1 on lattice contraction were seen during the first 72 h following casting, the effects on maintenance of cell viability are probably less important in promoting lattice contraction.
AB - The contraction of collagen lattices made with arterial smooth muscle cells was studied in medium MCDB 107 without serum or supplemented with 1% fetal bovine serum, plus insulin, transferrin, and low‐density lipoprotein. Under these conditions, smooth muscle cell mitogens including HBGF‐1 (aFGF), PDGF, and EGF stimulated contraction. Stimulation by HBGF‐1 was more profound than with other factors tested. HBGF‐1 stimulation of lattice contraction was blocked by protein synthesis inhibitors, but not by inhibitors of DNA synthesis. Histological observations indicated that HBGF‐1 also enhanced the maintenance of healthy cells in the lattice. Taken together, these observations suggest that HBGF‐1 stimulates lattice contraction, not by a mitogenic effect, but by stimulating synthesis of specific cellular proteins. Since the greatest effects of HBGF‐1 on lattice contraction were seen during the first 72 h following casting, the effects on maintenance of cell viability are probably less important in promoting lattice contraction.
UR - http://www.scopus.com/inward/record.url?scp=0026096846&partnerID=8YFLogxK
U2 - 10.1002/jcp.1041460115
DO - 10.1002/jcp.1041460115
M3 - 文章
C2 - 1703546
AN - SCOPUS:0026096846
SN - 0021-9541
VL - 146
SP - 110
EP - 116
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 1
ER -