TY - JOUR
T1 - Release of insulin-like growth factor carrier proteins by osteoblasts
T2 - Stimulation by estradiol and growth hormone
AU - Schmid, Christoph
AU - Ernst, Matthias
AU - Zapf, Jürgen
AU - Froesch, E. Rudolf
PY - 1989/4/28
Y1 - 1989/4/28
N2 - Osteoblast-like rat calvaria cells release specific insulin-like growth factor (IGF) carrier proteins (CPs). As analyzed by SDS-PAGE under nonreducing conditions, Western blotting and detection by 125I-IGFs, CPs migrating with the IGF-binding subunits of the major CP species of rat serum (42/45/49kDa) accumulate in cell culture medium. Treatment of the cells with growth hormone and estradiol increases the abundance of this glycosylated CP species. Since the two hormones were previously found to stimulate osteoblast replication via an IGF I-dependent mechanism, the data indicate that hormones may control local IGF action not only by regulating synthesis of IGFs and their receptors but also their presentation by CPs.
AB - Osteoblast-like rat calvaria cells release specific insulin-like growth factor (IGF) carrier proteins (CPs). As analyzed by SDS-PAGE under nonreducing conditions, Western blotting and detection by 125I-IGFs, CPs migrating with the IGF-binding subunits of the major CP species of rat serum (42/45/49kDa) accumulate in cell culture medium. Treatment of the cells with growth hormone and estradiol increases the abundance of this glycosylated CP species. Since the two hormones were previously found to stimulate osteoblast replication via an IGF I-dependent mechanism, the data indicate that hormones may control local IGF action not only by regulating synthesis of IGFs and their receptors but also their presentation by CPs.
UR - http://www.scopus.com/inward/record.url?scp=0024413229&partnerID=8YFLogxK
U2 - 10.1016/0006-291X(89)92502-3
DO - 10.1016/0006-291X(89)92502-3
M3 - Article
C2 - 2719697
AN - SCOPUS:0024413229
SN - 0006-291X
VL - 160
SP - 788
EP - 794
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -