Literature DB >> 21521798

Spermatogonial morphology and kinetics during testis development in mice: a high-resolution light microscopy approach.

Ana Luiza Drumond1, Marvin L Meistrich, Hélio Chiarini-Garcia.   

Abstract

Despite the knowledge of spermatogonial biology in adult mice, spermatogonial development in immature animals has not been fully characterized. Thus, the aim of this study was to evaluate the ontogeny of the morphological development of the spermatogonial lineage in C57BL/6 mouse testis, using high-resolution light microscopy. Spermatogonial morphology, chronology, and absolute number were determined for different ages postpartum (pp). The morphology of spermatogonia in immature mice was similar to that of adult spermatogonia, although their nuclear diameter was slightly smaller. The A(1) spermatogonia were first observed on day 2 pp, and only 24 h later, differentiating type A(3) and A(4) spermatogonia were observed in the seminiferous cords. This result indicated a shortening of the spermatogonial phase for immature mice of about ∼2.5 days when compared with adult mice and suggests that gonocytes and/or A(1) spermatogonia could directly become A(4) spermatogonia, skipping the developmental sequence of type A spermatogonia. These A(4) spermatogonia are functional as they develop into type B spermatogonia by day 5 pp. At day 8 pp, while differentiation to spermatocytes begins, the A(und) spermatogonia reach their maximal numbers, which are maintained through adulthood. The various details of the spermatogonial behavior in immature normal mice described in this study can be used as a baseline for further studies under experimental or pathological conditions.

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Year:  2011        PMID: 21521798     DOI: 10.1530/REP-10-0431

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  48 in total

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5.  The mTORC1 component RPTOR is required for maintenance of the foundational spermatogonial stem cell pool in mice†.

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8.  Rhox13 is required for a quantitatively normal first wave of spermatogenesis in mice.

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9.  STK31(TDRD8) is dynamically regulated throughout mouse spermatogenesis and interacts with MIWI protein.

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10.  Mammalian target of rapamycin complex 1 (mTORC1) Is required for mouse spermatogonial differentiation in vivo.

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