Meeting details menu

Meeting Authors
Meeting Abstracts
Keynote lectures
Oral communications
Poster presentations
Special symposia
Other

Acta Physiologica Congress

Back

Acta Physiologica 2008; Volume 194, Supplement 665
The 59th National Congress of the Italian Physiological Society
9/17/2008-9/19/2008
Cagliari, Italy


EXPRESSION OF PARP-1 AND OXIDATIVE STRESS-RELATED ENZYMES IN SERTOLI CELLS DURING RAT ONTOGENESIS
Abstract number: P130

SCARABELLI1 L, LANZA1 C, FUGASSA1 E, DEMORI1 I, ACCOMANDO1 R, PALMERO1 S

1Departement of Biology, University of [email protected]

Aim: 

The Sertoli cells play an essential role in determination of male somatic sex and spermatogenesis. The nuclear enzyme poly(ADP-ribose) polymerase-1 (PARP-1) is known to be involved in cell differentiation . In the whole rat testis and in rat germinal cells, PARP-1 has been proposed as a modulator of the changes in chromatin structure that takes place during spermatogenesis. Until now, PARP system has not been investigated in Sertoli cells. This study was aimed at investigating the expression pattern of PARP-1 and of oxidative stress-induced proteins in rat Sertoli cells during ontogenesis.

Methods: 

Sertoli cell primary cultures were obtained from immature and peripubertal rat testis. The transcript level of each gene (PARP-1, metallothionein-1 and 2, superoxide dismutase, catalase and glutathione-S-transferase) was quantified by real-time RT-PCR.

Results: 

For the first time, the expression of PARP-1 was quantified in rat Sertoli cells, and a modulation of PARP-1 expression during cell development was found. Constitutive expression of oxidative stress-related enzymes and metallothioneins are well evident at the early stages of testis development.

Conclusions: 

PARP-1 expression can be considered a sensitive marker of Sertoli cell differentiation during testis development.

To cite this abstract, please use the following information:
Acta Physiologica 2008; Volume 194, Supplement 665 :P130

Our site uses cookies to improve your experience.You can find out more about our use of cookies in our standard cookie policy, including instructions on how to reject and delete cookies if you wish to do so.

By continuing to browse this site you agree to us using cookies as described in our standard cookie policy .

CLOSE