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. 1966 Dec 1;31(3):381–396. doi: 10.1083/jcb.31.3.381

STUDIES OF SPERMIOGENESIS IN A NEMATODE, NIPPOSTRONGYLUS BRASILIENSIS

Mahendra P Jamuar 1
PMCID: PMC2107078  PMID: 6008326

Abstract

The fine structure of the developing spermatids and the mature sperm of Nippostrongylus brasiliensis was investigated. Immature spermatids are found at one end of the tubelike testis, and the mature sperm at the other. The spermatid has a prominent nucleus, with the chromatin clumped at the margin. It also contains a pair of centrioles, located near the nucleus. The cytoplasm is filled with ribosomal clusters, but it lacks an organized Golgi area or endoplasmic reticulum. Besides the normal mitochondria, the spermatid has specialized mitochondrionlike inclusions with dense matrix, few broad cristae, and a crystalloid structure always facing the nucleus. As spermiogenesis proceeds, the nucleus elongates, comes to lie at one end, and later evaginates to form a separate head structure, leaving the mitochondria and other cytoplasmic organelles in a broad cytoplasmic region. The nuclear material becomes filamentous and spiral, and the centrioles come to lie at one end near the junction of the head and the cytoplasmic portion of the sperm. Microtubules are found in the cytoplasmic region extending from the tubelike nucleus. The specialized mitochondria are about eighteen in number, and are arranged in rows in staggered groups of three around the microtubules in the cytoplasmic region. The mature sperm is aflagellate and lacks an acrosome. No movement of the sperm was ever observed.

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Selected References

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  1. ANDRE J. [Contribution to the knowledge of the chondriome. Study of its ultrastructural changes during spermatogenesis]. J Ultrastruct Res. 1962 May;Suppl 3:1–185. [PubMed] [Google Scholar]
  2. Alfert M., Geschwind I. I. A Selective Staining Method for the Basic Proteins of Cell Nuclei. Proc Natl Acad Sci U S A. 1953 Oct;39(10):991–999. doi: 10.1073/pnas.39.10.991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BAWA S. R. ELECTRON MICROSCOPE STUDY OF SPERMIOGENESIS IN A FIRE-BRAT INSECT, THRMOBIA DOMESTICA PACK. I. MATURE SPERMATOZOON. J Cell Biol. 1964 Dec;23:431–446. doi: 10.1083/jcb.23.3.431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BURGOS M. H., FAWCETT D. W. Studies on the fine structure of the mammalian testis. I. Differentiation of the spermatids in the cat (Felis domestica). J Biophys Biochem Cytol. 1955 Jul 25;1(4):287–300. doi: 10.1083/jcb.1.4.287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DASS C. M., RIS H. Submicroscopic organization of the nucleus during spermiogenesis in the grasshopper. J Biophys Biochem Cytol. 1958 Jan 25;4(1):129–132. doi: 10.1083/jcb.4.1.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. GALL J. G., BJORK L. B. The spermatid nucleus in two species of grasshopper. J Biophys Biochem Cytol. 1958 Jul 25;4(4):479–484. doi: 10.1083/jcb.4.4.479. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. KARNOVSKY M. J. Simple methods for "staining with lead" at high pH in electron microscopy. J Biophys Biochem Cytol. 1961 Dec;11:729–732. doi: 10.1083/jcb.11.3.729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. MCCUE J. F., THORSON R. E. A RAPID METHOD FOR COLLECTING LARGE NUMBERS OF INTESTINAL HELMINTHS. J Parasitol. 1963 Dec;49:997–997. [PubMed] [Google Scholar]
  10. MOSES M. J. Spermiogenesis in the crayfish (Procambarus clarkii). I. Structural characterization of the mature sperm. J Biophys Biochem Cytol. 1961 Jan;9:222–228. doi: 10.1083/jcb.9.1.222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. McLEISH J., SHERRATT H. S. The use of the Sakaguchi reaction for the cytochemical determination of combined arginine. Exp Cell Res. 1958 Jun;14(3):625–628. doi: 10.1016/0014-4827(58)90170-8. [DOI] [PubMed] [Google Scholar]
  12. PASTEELS J. Recherches sur le cycle germinal chez l'Ascaris; étude cytochimique des acides nucléiques dans l'oögénèse, la spermatogénès et le développement chez Parascaris equorum Goerze. Arch Biol (Liege) 1948;59(4):405–446. [PubMed] [Google Scholar]
  13. REGER J. F. Spermiogenesis in the tick, Amblyomma dissimili, as revealed by electron microscopy. J Ultrastruct Res. 1963 Jun;8:607–621. doi: 10.1016/s0022-5320(63)80059-3. [DOI] [PubMed] [Google Scholar]
  14. REGER J. F. THE FINE STRUCTURE OF SPERMATOZOA FROM THE ISOPOD ASELLUS MILITARIS (HAY). J Ultrastruct Res. 1964 Aug;11:181–192. doi: 10.1016/s0022-5320(64)80102-7. [DOI] [PubMed] [Google Scholar]
  15. SOTELO J. R., TRUJILLO-CENOZ O. Electron microscope study of the kinetic apparatus in animal sperm cells. Z Zellforsch Mikrosk Anat. 1958;48(5):565–601. doi: 10.1007/BF00342732. [DOI] [PubMed] [Google Scholar]
  16. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. J Biophys Biochem Cytol. 1958 Jul 25;4(4):475–478. doi: 10.1083/jcb.4.4.475. [DOI] [PMC free article] [PubMed] [Google Scholar]

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