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Original Paper
Cells Tissues Organs 2010;192:272–282
DOI: 10.1159/000317133
Nerve Growth Factor Promotes the
Survival of Goat Preantral Follicles
Cultured in vitro
R.N. Chaves
a
A.M.C.V. Alves
a
A.B.G. Duarte
a
V.R. Araújo
a
J.J.H. Celestino
a
M.H.T. Matos
a
C.A.P. Lopes
a
C.C. Campello
a
K.P.O. Name
b
S.N. Báo
b
J.R. Figueiredo
a
a
Laboratory of Manipulation of Oocytes and Preantral Follicles, Veterinary Faculty, State University of Ceara,
Fortaleza, and
b
Laboratory of Electron Microscopy, Department of Cell Biology, University of Brasilia, Brasilia, Brazil
developing follicles was significantly increased at all concen-
trations of NGF after 1 or 7 days of culture. We observed that
follicular diameter was greater at 1 and 10 ng/ml NGF after
culture for 7 days than at the other concentrations but was
similar to follicles cultured in -MEM+ alone. In conclusion,
NGF improved the survival of goat preantral follicles cul-
tured in vitro in a dose-dependent manner.
Copyright © 2010 S. Karger AG, Basel
Introduction
Understanding the signals responsible for the initia-
tion of folliculogenesis is an important step towards de-
veloping a successful in vitro system that promotes the
Key Words
Goat Ovarian follicles Nerve growth factor
Abstract
The aim of this study was to investigate the effects of nerve
growth factor (NGF) on the in vitro culture of goat preantral
follicles. Ovarian cortex fragments were cultured in -MEM+
supplemented with 0, 1, 10, 50, 100 or 200 ng/ml NGF for
1 or 7 days. Small fragments of noncultured ovarian tissue
as well as those cultured for 1 or 7 days were processed for
histology and transmission electron microscopy. The results
showed that after 1 or 7 days of culture at all concentrations
of NGF, except at 1 ng/ml after 1 day of culture, there was a
significant reduction in the percentage of normal follicles
compared to noncultured tissues. At higher NGF concentra-
tions (100 and 200 ng/ml) after 7 days of culture, there was a
significant reduction in the percentage of normal follicles
compared to tissues cultured in -MEM+ alone or at the oth-
er concentrations of NGF. It is important to note that ultra-
structural and fluorescent analyses confirmed only the in-
tegrity of follicles cultured with 1 ng/ml of NGF after 7 days.
In contrast to noncultured control tissues, the percentage of
Accepted after revision: March 19, 2010
Published online: June 26, 2010
Dr. Roberta Nogueira Chaves, Programa de Pós-Graduação em Ciências Veterinárias
Laboratório de Manipulação de Oócitos e Folículos Pré-Antrais
Universidade Estadual do Ceará, Campus do Itaperi, Av. Paranjana, 1700
Fortaleza, CE 60740-000 (Brazil)
Tel. +55 85 3101 9852, Fax +55 85 3101 9840, E-Mail rncvet @ gmail.com
© 2010 S. Karger AG, Basel
1422–6405/10/01924–0272$26.00/0
Accessible online at:
www.karger.com/cto
Abbreviations used in this paper
NGF nerve growth factor
TEM transmission electron microscopy
Trk tyrosine kinase