Abstract:Rey Vázquez, G., Da Cuña, R.H., Meijide, F.J., and Guerrero, G.A. 2012. Spermatogenesis and changes in testicular structure during the reproductive cycle in Cichlasoma dimerus (Teleostei, Perciformes). -Acta Zoologica (Stockholm) 93: 338-350.The present study aimed at analyzing spermatogenesis and the changes occurring in the testis throughout the reproductive cycle in the South American perciform fish Cichlasoma dimerus. Testes were studied using light and electron microscopy techniques. This species has an u… Show more
“…The testicular parenchyma of G. carapo displayed the germinal and interstitial compartments described in all vertebrates. As in other teleost fish (Nobrega and Quagio‐Grassiotto, ; Vazquez et al, ), the seminiferous tubules of this species contained spermatogenic cysts formed by Sertoli cells that envelop a group of synchronously developing germ cells. Histologically, the testis of G. carapo seem to correspond to the unrestricted spermatogonial testicular type, found in most teleosts, where spermatogonia reside along the testicular tubules (Grier et al, ; Grier, ).…”
Cell-cell interactions play essential roles in the regulation of gametogenesis. The involvement of junctional complexes in permeability barriers, for example, provides structural and physiological support for male germ-cell development. This study describes morphological characteristics of the reproductive system of Gymnotus carapo, a neo-tropical freshwater fish widely distributed in South and Central America, focusing on the detection of permeability barriers using morphological and biochemical approaches. Ultrastructural analysis of testes treated with the lanthanum nitrate exclusion technique showed that the tracer penetrated the interstitial compartment of the testis, surrounding and appearing within cysts containing spermatogonia and spermatocytes in early stages of meiosis, but was not detected in the spermatid cysts or inside the lumen of spermatogenic tubules. These results suggest the presence of a permeability barrier that is stabilized after meiosis is completed and serves to protect the haploid cells from the vascular system. In the spermatic-duct region, the tracer was obstructed near the lumen of the duct. Junctional complexes and focal tight junctions between adjacent cells were observed in the testis and spermatic duct. Freeze-fracture methods indeed confirmed the presence of tight junctions, which were visualized as parallel rows of individual particles between adjacent cells. More evidence supporting the existence of a permeability barrier was gathered from differences observed in the electrophoretic protein profiles of testis and spermatic-duct fluids compared to blood plasma. Together, these observations demonstrate the existence of a permeability barrier formed by tight junctions in the testis and spermatic duct of G. carapo.
“…The testicular parenchyma of G. carapo displayed the germinal and interstitial compartments described in all vertebrates. As in other teleost fish (Nobrega and Quagio‐Grassiotto, ; Vazquez et al, ), the seminiferous tubules of this species contained spermatogenic cysts formed by Sertoli cells that envelop a group of synchronously developing germ cells. Histologically, the testis of G. carapo seem to correspond to the unrestricted spermatogonial testicular type, found in most teleosts, where spermatogonia reside along the testicular tubules (Grier et al, ; Grier, ).…”
Cell-cell interactions play essential roles in the regulation of gametogenesis. The involvement of junctional complexes in permeability barriers, for example, provides structural and physiological support for male germ-cell development. This study describes morphological characteristics of the reproductive system of Gymnotus carapo, a neo-tropical freshwater fish widely distributed in South and Central America, focusing on the detection of permeability barriers using morphological and biochemical approaches. Ultrastructural analysis of testes treated with the lanthanum nitrate exclusion technique showed that the tracer penetrated the interstitial compartment of the testis, surrounding and appearing within cysts containing spermatogonia and spermatocytes in early stages of meiosis, but was not detected in the spermatid cysts or inside the lumen of spermatogenic tubules. These results suggest the presence of a permeability barrier that is stabilized after meiosis is completed and serves to protect the haploid cells from the vascular system. In the spermatic-duct region, the tracer was obstructed near the lumen of the duct. Junctional complexes and focal tight junctions between adjacent cells were observed in the testis and spermatic duct. Freeze-fracture methods indeed confirmed the presence of tight junctions, which were visualized as parallel rows of individual particles between adjacent cells. More evidence supporting the existence of a permeability barrier was gathered from differences observed in the electrophoretic protein profiles of testis and spermatic-duct fluids compared to blood plasma. Together, these observations demonstrate the existence of a permeability barrier formed by tight junctions in the testis and spermatic duct of G. carapo.
“…In a pilot study, 60 points proved sufficient to adequately determine the percentage of all cell types (we tested 45, 60, 75 and 90 points; p>0.05 for 60, 75 and 90). We followed the detailed histological description of C. dimerus testis by Rey Vázquez et al (2012) to correctly identify each cell type. Thereafter we calculated the percentage of type A and B spermatogonia, spermatocytes (primary and secondary combined), spermatids, spermatozoa and interstitial tissue.…”
Section: Quantification Of Testicular Cell Typesmentioning
“…Both types are present in the Perciform Order, however, the Type II is the most frequent, occurring in 29 from the 41 studied family, giving it the name of perciform spermatozoon (Mattei, ; Jamieson, ; Mattei, ; Abascal et al., ; Jamieson, ). However, against this tendency, the most species of the Cichlidae family, including C. kelberi in the present study, present the Type I (Mattei, ; Cruz‐Landim and Cruz‐Hofling, ; Jamieson, ; Silva and Godinho, ; Matos et al., ; Quagio‐Grassiotto et al., ; Jamieson, ; Vázquez et al., ).…”
Section: Discussionmentioning
confidence: 52%
“…Going on with Perciform, some of its representative can form one, two or even three lateral expansions from the flagellar membrane called ‘fins’ (Jamieson, ; Mattei, ). In the cichlids, as in C. kelberi, the fins are present in a pair, with lengths which vary according the specie (Cruz‐Landim and Cruz‐Hofling, ; Jamieson, ; Silva and Godinho, ; Matos et al., , ; Quagio‐Grassiotto et al., ; Vázquez et al., ). Nevertheless, it isn't one common family characteristic, because according Jamieson (), this structure was not observed in 13 species of Cichlidae, including some studied by Fishelson ().…”
Section: Discussionmentioning
confidence: 99%
“…Besides this three characteristic, the presence of cytoplasmic sheath and flagellum fins, observed in the C. kelberi spermatozoon, also are present isolated or together in some Cichlidae family representative (Cruz‐Landim and Cruz‐Hofling, ; Jamieson, ; Silva and Godinho, ; Matos et al., , ; Quagio‐Grassiotto et al., ; Vázquez et al., ), so, it can't be considered exclusive to the group. However all representative spermatozoon of Cichla genus described until this moment, present both the structure observed (Cruz‐Landim and Cruz‐Hofling, ; Quagio‐Grassiotto et al., ).…”
Summary
In the Neotropical cichlid Cichla kelberi the spermiogenesis appears to be of the cystic type and is characterized by gradual chromatin condensation in juxtaposed clusters, nuclear rotation (with the flagellum perpendicularly to the nucleus), and consequent nuclear fossa formation. Besides, there is cytoplasma migration to the nuclear base while eliminating the cytoplasmic residual mass. The heads of the spermatozoa are round, with approximately 1.87 μm in diameter; the nucleus has clusters juxtaposed of condensed chromatin. The nuclear fossa in single arc shape is moderate and slightly eccentric to the nuclear base. The midpiece is short and presents a cytoplasmic sheath, which dilated in its extremes. The mitochondria are spherical or slightly elongated. The flagellum presents the classical axoneme 9 + 2 and one pair of fins. The Type I C. kelberi spermatozoon has its flagellum perpendicularly positioned in relation to the nucleus base. The presence of only one flagellum characterize it as the basic spermatozoon in teleost, known as single anacrosomal aquasperm spermatozoon. Besides the patterns of previously cited characteristics between its representatives, the cytoplasmic sheath and flagellum fins presence can be consider as characteristics of the Cichla genus.
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