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      Ovarian nests in cultured females of the Siberian sturgeon Acipenser baerii (Chondrostei, Acipenseriformes) : ŻELAZOWSKA and FOPP-BAYAT

      1 , 2
      Journal of Morphology
      Wiley

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          Oogenesis in teleosts: how eggs are formed.

          One of the major objectives of the aquaculture industry is the production of a large number of viable eggs with high survival. Major achievements have been made in recent years in improving protocols for higher efficiency of egg production and viability of progeny. Main gaps remain, however, in understanding the dynamic processes associated with oogenesis, the formation of an egg, from the time that germ cells turn into oogonia, until the release of ova during spawning in teleosts. Recent studies on primordial germ-cells, yolk protein precursors and their processing within the developing oocyte, the deposition of vitamins in eggs, structure and function of egg envelopes and oocyte maturation processes, further reveal the complexity of oogenesis. Moreover, numerous circulating endocrine and locally-acting paracrine and autocrine factors regulate the various stages of oocyte development and maturation. Though it is clear that the major regulators during vitellogenesis and oocyte maturation are the pituitary gonadotropins (LH and FSH) and sex steroids, the picture emerging from recent studies is of complex hormonal cross-talk at all stages between the developing oocyte and its surrounding follicle layers to ensure coordination of the various processes that are involved in the production of a fertilizable egg. In this review we aim at highlighting recent advances on teleost fish oocyte differentiation, maturation and ovulation, including those involved in the degeneration and reabsorption of ovarian follicles (atresia). The role of blood-borne and local ovarian factors in the regulation of the key steps of development reveal new aspects associated with egg formation. Copyright 2009 Elsevier Inc. All rights reserved.
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            Mouse oocytes differentiate through organelle enrichment from sister cyst germ cells.

            Oocytes differentiate in diverse species by receiving organelles and cytoplasm from sister germ cells while joined in germline cysts or syncytia. Mouse primordial germ cells form germline cysts, but the role of cysts in oogenesis is unknown. We find that mouse germ cells receive organelles from neighboring cyst cells and build a Balbiani body to become oocytes, whereas nurselike germ cells die. Organelle movement, Balbiani body formation, and oocyte fate determination are selectively blocked by low levels of microtubule-dependent transport inhibitors. Membrane breakdown within the cyst and an apoptosis-like process are associated with organelle transfer into the oocyte, events reminiscent of nurse cell dumping in Drosophila We propose that cytoplasmic and organelle transport plays an evolutionarily conserved and functionally important role in mammalian oocyte differentiation.
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              Identification of germline stem cells in the ovary of the teleost medaka.

              Germline stem cells continually produce sperm in vertebrate testes, whereas there is no direct evidence showing that germline stem cells are present in adult vertebrate ovaries. By using transgenic methods and clonal analysis, we identified germline stem cells that supported oogenesis and the production of offspring in the ovaries of adult medaka fish. Early-stage germ cells were localized in clusters along interwoven threadlike cords of sox9b-expressing somatic cells (termed germinal cradles) where the germ cells developed. Germline stem cells gave rise to germ cells that divided to produce cysts, which then underwent cell death or separated to form follicles. Our results provide insight into the germline stem cell biology of medaka and provide a model system for studying vertebrate stem cell niches.
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                Author and article information

                Journal
                Journal of Morphology
                Journal of Morphology
                Wiley
                03622525
                October 2017
                October 2017
                July 06 2017
                : 278
                : 10
                : 1438-1449
                Affiliations
                [1 ]Department of Developmental Biology and Morphology of Invertebrates; Institute of Zoology and Biomedical Research, Jagiellonian University in Kraków, Gronostajowa 9; Kraków 30-387 Poland
                [2 ]Department of Ichthyology; Faculty of Environmental Science, University of Warmia and Mazury in Olsztyn, Oczapowskiego 5; Olsztyn 10-917 Poland
                Article
                10.1002/jmor.20723
                34ab0bf3-1456-4162-a10a-f70800b6a734
                © 2017

                http://doi.wiley.com/10.1002/tdm_license_1.1

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