Gametogenesis and Spawning Induction in Batissa violacea Lamarck, (1806) at Cagayan River, Philippines

Author(s):  
EUNICE A. LAYUGAN ◽  
SUSUMU SEGAWA ◽  
LIBERATO V. LAURETA ◽  
JESSE D. RONQUILLO

Batissaviolacea Lamarck (l806) locally known as “cabibi” is considered endemic in Cagayan River at Lallo, Philippines and the most expensive freshwater bivalve in the region. This study described through monthly histological examination the cytological characteristics of gametogenesis and sexual dimorphism of the gonad of B. violacea collected from the wild, and determined spawning response using serotonin. Eight category sizes of the species were established, and 10 samples from each size were processed. Gonads were preserved, and subjected for histological processes to confirm gametogenesis. Using descriptive data analysis, confirmation of the identified mature stage at 31-35 mm was further tested through induction of serotonin. Results showed progressive stages of sperm formation in male follicles. Follicles could be seen in clusters and identified as to their sizes from spermatogonia, spermatocytes, spermatids and spermatozoa. Growing female follicles appeared attached to a cytoplasmic stalk in different sizes and shapes. Initially male germ cells appeared tiny and became concentrated at the lumen in radiating bands as they become mature. Likewise, mature oocytes with enlarged nucleus and tiny nucleolus fill the center of the lumen of the female gonad was observed. B. violacea successfully spawn using either 0.2 ml or 0.5 ml earlier (0.21 hour) compared to 36.70 hour when no injection was administered. This is a first time report in the country along the possibility of breeding the species in captivity.Keywords: Aquatic ecology, Batissa violacea, gametogenesis, Cagayan River, induced spawning,experimental design, Cagayan river

Development ◽  
1982 ◽  
Vol 70 (1) ◽  
pp. 29-36
Author(s):  
V. Gremigni ◽  
M. Nigro ◽  
I. Puccinelli

The source and fate of blastema cells are important and still unresolved problems in planarian regeneration. In the present investigation we have attempted to obtain new evidence of cell dedifferentiation-redifferentiation by using a polyploid biotype of Dugesia lugubris s.1. This biotype is provided with a natural karyological marker which allows the discrimination of triploid embryonic and somatic cells from diploid male germ cells and from hexaploid female germ cells. Thanks to this cell mosaic we previously demonstrated that male germ cells take part in blastema formation and are then capable of redifferentiating into somatic cells. In the present investigation sexually mature specimens were transected behind the ovaries and the posterior stumps containing testes were allowed to regenerate the anterior portion of the body. Along with the usual hexaploid oocytes, a small percentage (3.2%) of tetraploid oocytes were produced from regenerated specimens provided with new ovaries. By contrast only hexaploid oocytes were produced from control untransected specimens. The tetraploid oocytes are interpreted as original diploid male germ cells which following the transection take part in blastema formation and then during regeneration redifferentiate into female germ cells thus doubling their chromosome number as usual for undifferentiated cells entering the female gonad in this biotype.


2020 ◽  
Vol 21 (22) ◽  
pp. 8494
Author(s):  
Virginie Barraud-Lange ◽  
Côme Ialy-Radio ◽  
Céline Chalas ◽  
Isabelle Holtzmann ◽  
Jean-Philippe Wolf ◽  
...  

We have previously shown, using antibodies, that the sperm alpha6beta1 integrin is involved in mouse gamete fusion in vitro. Here we report the conditional knockdown of the sperm Itgb1 gene. It induced a drastic failure of sperm fusogenic ability with sperm accumulation in the perivitelline space of in vitro inseminated oocytes deleted or not for the Itgb1 gene. These data demonstrate that sperm, but not oocyte, beta1 integrin subunit is involved in gamete adhesion/fusion. Curiously, knockdown males were fertile in vivo probably because of the incomplete Cre-mediated deletion of the sperm Itgb1 floxed gene. Indeed, this was shown by Western blot analysis and confirmed by both the viability and litter size of pups obtained by mating partially sperm Itgb1 deleted males with females producing completely deleted Itgb1 oocytes. Because of the total peri-implantation lethality of Itgb1 deletion in mice, we assume that sperm that escaped the Itgb1 excision seemed to be preferentially used to fertilize in vivo. Here, we showed for the first time that the deletion, even partial, of the sperm Itgb1 gene makes the sperm unable to normally fertilize oocytes. However, to elucidate the question of the essentiality of its role during fertilization, further investigations using a mouse expressing a recombinase more effective in male germ cells are necessary.


Endocrinology ◽  
2012 ◽  
Vol 153 (5) ◽  
pp. 2466-2473 ◽  
Author(s):  
Benoit Souquet ◽  
Sophie Tourpin ◽  
Sébastien Messiaen ◽  
Delphine Moison ◽  
René Habert ◽  
...  

The mechanisms regulating the entry into meiosis in mammalian germ cells remain incompletely understood. We investigated the involvement of the TGF-β family members in fetal germ cell meiosis initiation. Nodal, a member of the TGF-β family, and its target genes are precociously expressed in embryonic gonads and show sexual dimorphism in favor of the developing testis. Nodal receptor genes, Acvr2a and Acvr2b, Alk4, and Tdgf1/Cripto, were identified in male germ cells. Nodal itself, Tdgf1, and Lefty1 and Lefty2 are targets of Nodal signaling and were all found specifically expressed in male germ cells. To elucidate the role of this signaling pathway, activin-like kinases that mediate TGF-β/Nodal/activin signaling were inhibited in 11.5 d postconception testis in organotypic culture. Activin-like kinases inhibition disrupted normal male germ cell development and induced germ cell entry into meiosis such as that observed in female germ cells at the equivalent stage. Interestingly Stra8, the gatekeeper of the mitotic/meiotic switch, was induced independently of any change of either Cyp26b1 or Fgf9 expression, the two genes currently identified as testicular meiotic inhibitors. On the other hand, recombinant Nodal significantly dampened Stra8 expression and germ cell meiosis in cultured 11.5 d postconception ovaries. Our results allowed us to propose for the first time an autocrine role of Nodal during the development of germ cells and indicate that members of the TGB-β family may reinforce the male fate and prevent meiosis in embryonic germ cells.


iScience ◽  
2021 ◽  
pp. 102890
Author(s):  
Ryuki Shimada ◽  
Hiroko Koike ◽  
Takamasa Hirano ◽  
Yuzuru Kato ◽  
Yumiko Saga

1956 ◽  
Vol 2 (4) ◽  
pp. 123-128 ◽  
Author(s):  
H. W. Beams ◽  
T. N. Tahmisian ◽  
R. L. Devine ◽  
Everett Anderson

The dictyosome (Golgi body) in the secondary spermatocyte of the cricket appears in electron micrographs as a duplex structure composed of (a) a group of parallel double-membraned lamellae and (b) a group of associated vacuoles arranged along the compact lamellae in a chain-like fashion. This arrangement of ultramicroscopic structure for the dictyosomes is strikingly comparable to that described for the Golgi apparatus of vertebrates. Accordingly, the two are considered homologous structures. Associated with the duplex structure of the dictyosomes is a differentiated region composed of small vacuoles. This is thought to represent the pro-acrosome region described in light microscope preparations. In the spermatid the dictyosomes fuse, giving rise to the acroblast. Like the dictyosomes, the acroblasts are made up of double-membraned lamellae and associated vacuoles. In addition, a differentiated acrosome region is present which, in some preparations, may display the acrosome vacuole and granule. Both the dictyosomes and acroblasts are distinct from mitochondria.


2001 ◽  
Vol 20 (6) ◽  
pp. 1289-1299 ◽  
Author(s):  
Michael R. Bösl ◽  
Valentin Stein ◽  
Christian Hübner ◽  
Anselm A. Zdebik ◽  
Sven-Eric Jordt ◽  
...  

Nature ◽  
1953 ◽  
Vol 172 (4380) ◽  
pp. 690-690 ◽  
Author(s):  
JOHN R. BAKER

Sign in / Sign up

Export Citation Format

Share Document