TY - JOUR
T1 - Glomerulosclerosis in mice transgenic for growth hormone. Increased mesangial extracellular matrix is correlated with kidney mRNA levels
AU - Doi, Toshio
AU - Striker, Liliane J.
AU - Kimata, Koji
AU - Peten, Emanuel P.
AU - Yamada, Yoshihiko
AU - Striker, Gary E.
PY - 1991/5/1
Y1 - 1991/5/1
N2 - Mice transgenic for growth hormone (GH) develop progressive glomerulosclerosis. The compositions of kidney extracellular matrix (ECM) and ECM mRNA were examined. The glomerulosclerotic areas in GH mice contained types I and IV collagen, laminin, and basement membrane heparan sulfate proteoglycan (HSPG), which increased with age. The type IV collagen, laminin B2, and HSPG mRNA levels in GH mice, measured by a solution hybridization RNase protection assay, were increased over normal littermates. These findings suggest that the accumulation of ECM components in the glomeruli of GH mice is regulated at the transcriptional level and that glomerulosclerosis is, in part, due to the excess production of ECM rather than simply a reduction in its turnover. The glomerular lesions in GH mice resemble diabetic nephropathy and may allow further dissection of the molecular basis of certain forms of glomerulosclerosis.
AB - Mice transgenic for growth hormone (GH) develop progressive glomerulosclerosis. The compositions of kidney extracellular matrix (ECM) and ECM mRNA were examined. The glomerulosclerotic areas in GH mice contained types I and IV collagen, laminin, and basement membrane heparan sulfate proteoglycan (HSPG), which increased with age. The type IV collagen, laminin B2, and HSPG mRNA levels in GH mice, measured by a solution hybridization RNase protection assay, were increased over normal littermates. These findings suggest that the accumulation of ECM components in the glomeruli of GH mice is regulated at the transcriptional level and that glomerulosclerosis is, in part, due to the excess production of ECM rather than simply a reduction in its turnover. The glomerular lesions in GH mice resemble diabetic nephropathy and may allow further dissection of the molecular basis of certain forms of glomerulosclerosis.
UR - http://www.scopus.com/inward/record.url?scp=0025907477&partnerID=8YFLogxK
U2 - 10.1084/jem.173.5.1287
DO - 10.1084/jem.173.5.1287
M3 - Article
C2 - 2022927
AN - SCOPUS:0025907477
SN - 0022-1007
VL - 173
SP - 1287
EP - 1290
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 5
ER -