Literature DB >> 24202483

GTH-cells in the pituitary of the African catfish, Clarias gariepinus, during gonadal maturation: an immuno-electron microscopical study.

M A Zandbergen1, C A van Branden, R W Schulz, J Janssen-Dommerholt, J M Ruijter, H J Goos, J Peute.   

Abstract

In an ultrastructural immunocytochemical study we investigated the development of the gonadotropic cells in the pituitary of two to six months old male African catfish in relation to testicular development. In this period, pituitary and testicular tissue samples were collected on five occasions (groups I-V). Blood samples could only be taken from the fish in groups III-V. The testicular development was divided in three stages i.e., immature (only spermatogonia, group I), early (spermatogonia and spermatocytes, groups II and III) and advanced (all germ cell stages including spermatozoa, groups IV and V) spermatogenesis. 11-Ketotestosterone blood levels were low, except for the last group. Antisera were raised against the complete catfish α,βGTH-II, as well as to the separate α- and β-subunits of catfish GTH-II. In the proximal pars distalis of immature fish, undifferentiated cells, somatotrops, putative thyrotrops (pTSH) and putative gonadotrops (pGTH) were found. In the two latter, secretory granules were labeled with anti-αGTH, but not with anti-βGTH-II. pTSH- and pGTH-cells were distinguished on the basis of the size of their secretory granules. During early spermatogenesis, two classes of putative gonadotrops could be distinguished. One type had the same immunocytochemical and ultrastructural characteristics as in immature fish; the secretory granules in the second cell type, which was more abundant, were also immunopositive for anti-βGTH-II. The mean volume of the secretory granules in these GTH-II cells was three times larger than that in the early appearing pGTH-cells. In addition, the later appearing GTH-II cells contained large inclusions, known as globules. These structures labeled with anti-αβGTH-II and with anti-βGTH-II, but not with anti-αGTH. It is assumed that the globules are involved in a differential storage and/or breakdown of the GTH-II subunits. During advanced spermatogenesis the two gonadotropic cell types could still be distinguished, but the early appearing pGTH-cell type was scarce. The present observations permit the conclusion that the early appearing cells may be GTH-I cells. However, definitive proof about their identity depends on the availability of antibodies or cDNA probes specific for GTH-I.

Entities:  

Year:  1993        PMID: 24202483     DOI: 10.1007/BF00004573

Source DB:  PubMed          Journal:  Fish Physiol Biochem        ISSN: 0920-1742            Impact factor:   2.794


  15 in total

1.  Salmonid pituitary gonadotrophs. II. Ontogeny of GTH I and GTH II cells in the rainbow trout (Salmo gairdneri irideus).

Authors:  M Nozaki; N Naito; P Swanson; W W Dickhoff; Y Nakai; K Suzuki; H Kawauchi
Journal:  Gen Comp Endocrinol       Date:  1990-03       Impact factor: 2.822

2.  Salmonid pituitary gonadotrophs. I. Distinct cellular distributions of two gonadotropins, GTH I and GTH II.

Authors:  M Nozaki; N Naito; P Swanson; K Miyata; Y Nakai; Y Oota; K Suzuki; H Kawauchi
Journal:  Gen Comp Endocrinol       Date:  1990-03       Impact factor: 2.822

3.  Isolation and characterization of two distinct gonadotropins from chum salmon pituitary glands.

Authors:  K Suzuki; H Kawauchi; Y Nagahama
Journal:  Gen Comp Endocrinol       Date:  1988-08       Impact factor: 2.822

4.  Stereological estimation of the volume-weighted mean volume of arbitrary particles observed on random sections.

Authors:  H J Gundersen; E B Jensen
Journal:  J Microsc       Date:  1985-05       Impact factor: 1.758

5.  Application of cryosubstitution in neurohormone- and neurotransmitter-immunocytochemistry.

Authors:  M A Zandbergen; J Peute; A J Verkley; H J Goos
Journal:  Histochemistry       Date:  1992

6.  Purification, characterization, and molecular cloning of gonadotropin subunits of silver carp (Hypophthalmichthys molitrix).

Authors:  Y S Chang; C J Huang; F L Huang; C S Liu; T B Lo
Journal:  Gen Comp Endocrinol       Date:  1990-04       Impact factor: 2.822

7.  Serum levels of 11-oxotestosterone in male and 17 beta-estradiol in female rainbow trout (Salmo gairdneri) during the first reproductive cycle.

Authors:  R Schulz
Journal:  Gen Comp Endocrinol       Date:  1984-10       Impact factor: 2.822

8.  Steroid metabolism in the testes of the African catfish, Clarias gariepinus (Burchell), during spawning season, under natural conditions and kept in ponds.

Authors:  W G Schoonen; J G Lambert
Journal:  Gen Comp Endocrinol       Date:  1986-01       Impact factor: 2.822

9.  Separation of gonadotropic fractions with different species specificities from tuna pituitaries.

Authors:  H Ando; S Ishii
Journal:  Gen Comp Endocrinol       Date:  1988-05       Impact factor: 2.822

10.  Isolation and characterization of subunits from two distinct salmon gonadotropins.

Authors:  K Suzuki; H Kawauchi; Y Nagahama
Journal:  Gen Comp Endocrinol       Date:  1988-08       Impact factor: 2.822

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