Literature DB >> 26413404

Testicular structure in three viviparous species of teleosts in the genus Jenynsia (Anablepidae).

V H Martínez1, G Monasterio de Gonzo1, M C Uribe2, H J Grier3.   

Abstract

Histological structure of the testes and development of spermatozoa in Jenynsia species is described using light, scanning and transmission electron microscopy. The testis type is restricted spermatogonial, wherein spermatogonia are restricted to the distal ends of lobules, typical of the Atherinomorpha, and spermatogenesis is continuous throughout the year in wild-caught fish. Within the testicular lobes there are lobular germinal compartments wherein the functional units are spermatocysts, whose borders are formed by Sertoli cells. Spermatocysts may contain meiotic primary spermatocytes, secondary spermatocytes, spermatids, undergoing spermiogenesis, or spermatozoa. Spermatocysts with later stages of developing sperm are located proximal to the testicular ducts. During spermiogenesis, spermatid nuclei become elongated. As this occurs, the nucleus develops a deep, central fossa that contains the centriolar complex. As the flagellum grows, enlarging spermatid mitochondria migrate posteriorly alongside the flagellum but remain separated from it by the cytoplasmatic canal, an indentation of the plasma membrane. Between the enlarged mitochondria and plasma membrane, a sub-mitochondrial net develops. In longitudinal sections, the enlarged mitochondria are stacked in a zig-zag fashion, and in transverse sections they appear as a ring surrounding the flagellum, but separated from it by the cytoplasmic canal. Spermatozoa of the 3 jenynsiid species have an introsperm complex composed of a long mid-piece whose flagellum has a single "wing." Within the efferent ducts and the tubular gonopodium, sperm are lightly packed in a side by side fashion which facilitates their transfer into the female reproductive tract. This study presents detailed descriptions of testicular organization and cytological characterization of the stages of spermatozoa differentiation in 3 species of Jenynsia from northwestern Argentina (J. alternimaculata, J. multidentata and J. maculata), in order to contribute to the understanding of testicular structure and development of spermatozoa in the context of evolution of viviparity in this fish lineage.

Entities:  

Keywords:  Jenynsids; spermatogenesis; spermatozoon; testis; viviparous teleost

Year:  2015        PMID: 26413404      PMCID: PMC4581060          DOI: 10.4161/21565562.2014.983399

Source DB:  PubMed          Journal:  Spermatogenesis        ISSN: 2156-5554


  13 in total

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Authors:  I Quagio-Grassiotto; E D Carvalho
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4.  Evolution and phylogeny of gonad morphology in bony fishes.

Authors:  Lynne R Parenti; Harry J Grier
Journal:  Integr Comp Biol       Date:  2004-11       Impact factor: 3.326

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Authors:  H J Grier
Journal:  J Ultrastruct Res       Date:  1973-10

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Journal:  Z Zellforsch Mikrosk Anat       Date:  1967

7.  Spermiogenesis in the teleost Gambusia affinis with particular reference to the role played by microtubules.

Authors:  H J Grier
Journal:  Cell Tissue Res       Date:  1975-12-29       Impact factor: 5.249

8.  Sperm morphology and IMP distribution in membranes of spermatozoa of cyprinid fishes II.

Authors:  T Ohta; M Matsuda
Journal:  Cell Struct Funct       Date:  1995-08       Impact factor: 2.212

9.  Cyclic changes in fine structure of the epithelium lining the ovary of the viviparous teleost, Cymatogaster aggregata (Perciformes: Embiotocidae).

Authors:  D M Gardiner
Journal:  J Morphol       Date:  1978-06       Impact factor: 1.804

10.  Involvement of the gonadal germinal epithelium during sex reversal and seasonal testicular cycling in the protogynous swamp eel, Synbranchus marmoratus Bloch 1795 (Teleostei, Synbranchidae).

Authors:  F Lo Nostro; H Grier; L Andreone; G A Guerrero
Journal:  J Morphol       Date:  2003-07       Impact factor: 1.804

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