Platelet-derived growth factor-BB stimulates hypertrophy of peritubular smooth muscle cells from rat testis in primary cultures

被引:23
作者
Chiarenza, C
Filippini, A
Tripiciano, A
Beccari, E
Palombi, F
机构
[1] Univ Roma La Sapienza, CNR, Dept Histol & Med Embryol, I-00161 Rome, Italy
[2] Univ Roma La Sapienza, CNR, Ctr Acidi Nucl, I-00161 Rome, Italy
关键词
D O I
10.1210/en.141.8.2971
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The tunica propria of seminiferous tubules contains a particular type of smooth muscle cell (myoid cells) arranged in a contractile epithelioid layer that is responsible for sperm and tubular fluid flow. Unlike other types of smooth muscle (SM) cells, highly purified populations of peritubular smooth muscle cells (PSMC) survive and maintain their contractile phenotype in primary cultures in controlled conditions. We used this culture model to investigate the response of the SM contractile phenotype to prolonged exposure to platelet-derived growth factor (PDGF), one of the main factors involved in vascular SM pathologies. We observed that 4-day continuous exposure of PSMC to PDGF-BB at nanomolar concentrations in plain medium enhances contractile phenotype traits and induces cell hypertrophy without inducing proliferation. In Northern and Western blotting experiments, SM-alpha-actin transcript and protein were found to be markedly increased in the PDGF-BB-treated samples, which is in line with the formation of conspicuous SM-ol-actin-containing stress fibers. Moreover, binding sites for endothelin-l were increased, and the calcium response to the contractile agonist, determined in single fura-a-loaded cells, was enhanced. In response to PDGF-BB, the cells underwent immediate, transient contraction, as seen in a scanning electron microscope, followed by a gradual increase in size, as evaluated by cytofluorometry, and enhancement of protein synthesis. The observed pattern of response to PDGF-BB was not accompanied by cell proliferation, as assessed by [H-3]thymidine incorporation and direct cell counts. Unlike other SM cell types, in which proliferation and loss of contractile traits are induced by PDGF, chronic treatment of PSMC with this growth factor results in hypertrophy rather than hyperplasia.
引用
收藏
页码:2971 / 2981
页数:11
相关论文
共 50 条
[1]   Endothelin-1 induces an increase in total protein synthesis and expression of the smooth muscle alpha-actin gene in vascular smooth muscle cells [J].
Andrawis, NS ;
Wang, EH ;
Abernethy, DR .
LIFE SCIENCES, 1996, 59 (07) :523-528
[2]   VASOCONSTRICTION - A NEW ACTIVITY FOR PLATELET-DERIVED GROWTH-FACTOR [J].
BERK, BC ;
ALEXANDER, RW ;
BROCK, TA ;
GIMBRONE, MA ;
WEBB, RC .
SCIENCE, 1986, 232 (4746) :87-90
[3]   PLATELET-DERIVED GROWTH-FACTOR REGULATES ACTIN ISOFORM EXPRESSION AND GROWTH-STATE IN CULTURED RAT AORTIC SMOOTH-MUSCLE CELLS [J].
BLANK, RS ;
OWENS, GK .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 142 (03) :635-642
[4]  
BLANK RS, 1988, J CELL BIOL, V107, P229
[5]   A novel role for the cyclin-dependent kinase inhibitor p27Kip1 in angiotensin II-stimulated vascular smooth muscle cell hypertrophy [J].
Braun-Dullaeus, RC ;
Mann, MJ ;
Ziegler, A ;
von der Leyen, HE ;
Dzau, VJ .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (06) :815-823
[6]   SELECTIVE-INHIBITION OF THE PLATELET-DERIVED GROWTH-FACTOR SIGNAL-TRANSDUCTION PATHWAY BY A PROTEIN-TYROSINE KINASE INHIBITOR OF THE 2-PHENYLAMINOPYRIMIDINE CLASS [J].
BUCHDUNGER, E ;
ZIMMERMANN, J ;
METT, H ;
MEYER, T ;
MULLER, M ;
REGENASS, U ;
LYDON, NB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2558-2562
[7]  
CHUA RH, 1992, AM J PHYSIOL, V262, pE412
[8]  
CORJAY MH, 1989, J BIOL CHEM, V264, P10501
[9]   PLATELET-DERIVED GROWTH FACTOR-INDUCED DESTABILIZATION OF SMOOTH-MUSCLE ALPHA-ACTIN MESSENGER-RNA [J].
CORJAY, MH ;
BLANK, RS ;
OWENS, GK .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 145 (03) :391-397
[10]   CELLULAR ARCHITECTURE OF THE LAMINA PROPRIA OF HUMAN SEMINIFEROUS TUBULES [J].
DAVIDOFF, MS ;
BREUCKER, H ;
HOLSTEIN, AF ;
SEIDL, K .
CELL AND TISSUE RESEARCH, 1990, 262 (02) :253-261