Published August 2018 | Version v1
Journal article

HIF involvement in the regulation of rat Sertoli cell proliferation by FSH

  • 1. Centro de Investigaciones Endocrinológicas <sup>D</sup>r. César Bergadá<sup> </sup>(CEDIE) CONICET-FEI-División de Endocrinología, Hospital de Niños Ricardo Gutiérrez, Gallo 1330, Buenos Aires, C1425EFD (Argentina)

Description

Highlights: • FSH increases HIF transcriptional activity in immature Sertoli cells. • FSH upregulates CCND1 expression in a HIF-dependent manner. • FSH upregulates c-Myc transcriptional activity in a HIF-dependent manner. • HIFs might be involved in the regulation of Sertoli cell proliferation by FSH. The final number of Sertoli cells reached during the proliferative periods determines sperm production capacity in adulthood. It is well known that FSH increases the rate of proliferation of Sertoli cells; however, little is known about the transcription factors that are activated by the hormone in order to regulate Sertoli cell proliferation. On the other hand, Hypoxia Inducible Factors (HIFs) are master regulators of cell growth. HIFs are dimers of HIF-β and HIF-α subunits. Considering that HIF-β is constitutively expressed, HIF transcriptional activity is regulated through the abundance of HIF-α subunits. To date, three HIF-α isoforms have been described. The association of the different HIF-α subunits with HIF-β subunit constitutes three active transcription factors —HIF-1, HIF-2 and HIF-3— which interact with consensus hypoxia-response elements in the promoter region of target genes. Hypoxia has been classically considered the main stimulus that increases HIF transcriptional activity, however, regulation by hormones under normoxic conditions was also demonstrated. The aim of this work has been to investigate whether HIFs participate in the regulation of rat Sertoli cell proliferation by FSH. Sertoli cells obtained from 8-day old rats were cultured in the absence or presence of FSH. It has been observed that FSH increases HIF transcriptional activity and HIF-2α mRNA levels without modifying either HIF-1α or HIF-3α expression. Incubations with FSH have been also performed in the absence or presence of a pharmacological agent that promotes HIF-α subunit degradation, LW6. It has been observed that LW6 inhibits the FSH effect on proliferation, CCND1 expression and c-Myc transcriptional activity. Altogether, these results suggest that HIFs might be involved in the regulation of Sertoli cell proliferation by FSH.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2018.05.206

Additional details

Identifiers

DOI
10.1016/j.bbrc.2018.05.206;
PII
S0006291X1831297X;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
502
Journal Issue
4
Journal Page Range
p. 508-514
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
53054198
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ANOXIA; CELL PROLIFERATION; FSH; MESSENGER-RNA; RATS; SPERMATOZOA; TRANSCRIPTION FACTORS
Descriptors DEC
ANIMALS; GAMETES; GERM CELLS; GONADOTROPINS; HORMONES; MAMMALS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; PEPTIDE HORMONES; PITUITARY HORMONES; PROTEINS; RNA; RODENTS; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2018 Elsevier Inc. All rights reserved.