Degeneration of Sertoli and Spermatogenic Cells in Homozygous and Heterozygous Weaver Mice

References

• Bryan J. H. D. Spermatogenesis revised. I. On the presence of multinucleate spermatogenic cells in the seminiferous epithelium of the mouse. Z Zellforsch Microsk. Anat. 1971; 112: 333–349
   PubMedGoogle Scholar
• Bryan J. H. D. Spermatogenesis revisited. III. The course of spermatogenesis in a male-sterile pink-eyed mutant type in the mouse. Cell Tissue Res. 1977; 180: 173–186
   PubMed Web of Science ®Google Scholar
• Eisenberg B., Messer A. Tonic/clonic seizures in a mouse mutant carrying the weaver gene. Neurosci. Lett. 1989; 96: 168–172
   PubMedGoogle Scholar
• Fawcett D. W. Ultrastructure and function of the Sertoli cell. Handbook of Physiology, v. 5, R. O. Greep, E. B. Atwood. Am. Physiol. Soc., Washington, D. C. 1975; 21–53
   Google Scholar
• Ghetti B., Triarhou L. C. Combined degeneration of cerebellar granule cells and of midbrain dopamine neurons in the weaver mutant mouse. Advances in Parkinson Research, W. J. Weiner, F. F. Hefti. Futura Publishing Co., Mount Kisco, NY 1992; 375–388
   Google Scholar
• Goldowitz D., Mullen R. J. Granule cell as a site of a gene action in the weaver mouse cerebellum: evidence from heterozygous mutant chimeras. J. Neurosci. 1982; 2: 1474–1485
   PubMed Web of Science ®Google Scholar
• Green M. C. Catalog of mutant genes on polymorphic loci. Genetic variants and strains of the laboratory mouse, M. C. Green. Gustav Fisher Verlag, New York 1981; 8–278
   Google Scholar
• Gupta M., Felten D. L., Ghetti B. Selective loss of monoaminergic neurons in weaver mutant mice—an immunocytochemical study. Brain Res. 1987; 402: 379–382
   PubMedGoogle Scholar
• Handel M. A. Effects of colchicine on spermatogenesis in the mouse. J. Embryol. Exp. Morph. 1979; 51: 73–83
   PubMedGoogle Scholar
• Hugenholtz A. P. Mouse News Lett. 1984; 71: 34–35
   Google Scholar
• Hunt D. M., Johnson D. R. Abnormal spermiogenesis in two pink-eyed sterile mutants in the mouse. J. Embryol. Exp. Morphol. 1971; 26: 111–121
   PubMedGoogle Scholar
• Johnson D. R. Multinucleate spermatids in the mouse. A quantitative electron microscope study. Cell Tiss. Res. 1974; 150: 323–329
   PubMedGoogle Scholar
• Kaya M. Sertoli cells and various types of multinucleates in the rat seminiferous tubules following temporary ligation of the testicular artery. J. Anat. 1986; 144: 15–29
   PubMedGoogle Scholar
• Krzanovska H. (1971) Influence of Y chromosome on fertility in mice. The Genetics of the Spermatozoa. Proceedings of the International Symposium held at University of Edinburgh. Aug. 16–20, 1971, R. A. Beatty, S. Gluecksohn-Waelsch
   Google Scholar
• MacGregor G. R., Russell L. D., Van Beek M. E. A. B., Hanten G. R., Kovac M. J., Kozak C. A., Meistrich M. A., Overbeek P. A. Symplastic spermatids (sys), a recessive insertional mutation in mice causing a defect in spermatogenesis. Proc. Natl. Acad. Sci. USA 1990; 87: 5016–5020
   PubMedGoogle Scholar
• Meistrich M. L., Trostle-Weige P. K., Russell L. D. Abnormal manchette development in spermatids of azh/azh mutant mice. Am. J. Anat. 1990; 188: 74–86
   PubMedGoogle Scholar
• Neter J., Wasserman W., Kutner M. H. Applied Linear Statistical Models, 2d Edition. Richard D. Irvin, Inc., Homewood, Ill. 1985
   Google Scholar
• Oettle A. G., Harrison R. G. The histological changes produced in the rat testis by temporary and permanent occlusion of the testicular artery. J. Path. Bacteriol. 1952; 64: 273–297
   PubMedGoogle Scholar
• Rakic P., Sidman R. L. Sequence of developmental abnormalities leading to granule cell deficit in cerebellar cortex in weaver mutant mice. J. Comp. Neur. 1973a; 152: 103–132
   PubMed Web of Science ®Google Scholar
• Rakic P., Sidman R. L. Organization of cerebellar cortex secondary to deficit of granule cells in weaver mutant mice. J. Comp. Neur. 1973b; 152: 103–132
   PubMed Web of Science ®Google Scholar
• Russell L. D., Vogl A. W., Weber J. E. Actin localization in male germ cell intercellular bridges in the rat and ground squirrel and disruption of bridges by cytochalasin D. Am. J. Anat. 1987; 180: 25–40
   PubMedGoogle Scholar
• Russell L. D., Bartke A., Goh J. C. Postnatal development of the Sertoli cell barrier, tubular lumen and cytoskeleton of Sertoli and myoid cells in the rat, and their relationship to tubular fluid secretion and flow. Amer. J. Anat. 1989; 184: 179–189
   PubMedGoogle Scholar
• Russell L. D., Ettlin R. A., Sinha Hikim A. P., Clegg E. D. Histological and Histopathological Evaluation of the Testis. Cache River Press, Florida 1990
   Google Scholar
• Russell L. D., Russell J. A., MacGregor G. R., Meistrich M. L. Linkage of manchette microtubules to the nuclear envelope and observations of the role of the manchette in nuclear shaping during spermiogenesis in rodents. Am J. Anat. 1991a; 192: 97–120
   PubMedGoogle Scholar
• Russell L. D., Sinha Hikim A. P., Overbeek P. A., MacGregor G. R. Testis structure in the sys (symplastic spermatids) mouse. Am. J. Anat. 1991b; 192: 169–182
   PubMedGoogle Scholar
• SAS Institute Inc. SAS/STAT User's Guide, Release 6.03 edn, N. C. Cary. SAS Institute Inc. 1988
   Google Scholar
• Schmidt M. J., Sawyer B. D., Perry K. W., Fuller R. W, Foreman M. M., Ghetti B. Dopamine deficiency in the weaver mutant mouse. J. Neurosc. 1982; 2: 376–380
   PubMed Web of Science ®Google Scholar
• Seifried T. H. Convulsive disorders. The Mouse in Biomedical Research, H. S. Foster, J. D. Small, J. G. Fox. Academic, New York 1982; Vol. 4: 97–124
   Google Scholar
• Sidman R. L., Green M. C., Appel S. H. Catalog of the Neurological Mutants of the Mouse. Harvard University Press, Cambridge 1965
   Google Scholar
• Singh S. K., Abe K. Light and electron microscopic observations of giant cells in the mouse testis after efferent duct ligation. Arch. Histol. Jpn. 1987; 50: 579–585
   PubMedGoogle Scholar
• Sotelo C. Anatomical, physiological and biochemical studies of the cerebellum from mutant mice. II. Morphological studies of cerebellar cortical neurons and circuits in the weaver mouse. Brain Res. 1975; 94: 19–44
   PubMedGoogle Scholar
• Sotelo C. Mutant mice and the formation of the cerebellar circuitry. Trends Neurosci. 1980; 3: 33–36
   Google Scholar
• Steinberger E., Tjioe D. Y. Spermatogenesis in rat testes after experimental ischaemia. Fert, and Steril. 1969; 20: 639–649
   PubMed Web of Science ®Google Scholar
• Tao J., Critser E. S., Critser J. K. Evaluation of mouse sperm acrosomal status and viability by flow cytometry. Mol. Reprod. Develop. 1993; 36: 183–194
   PubMedGoogle Scholar
• Triarhou L. C., Ghetti B. Neuroanatomical substrate of behavioral impairment in weaver mutant mice. Exp. Brain Res. 1987; 68: 434–436
   PubMedGoogle Scholar
• Triarhou L. C., Norton J., Ghetti B. Mesencephalic dopamine cell deficit involves areas A8, A9 and A10 in weaver mutant mice. Exp. Brain Res. 1988; 70: 256–265
   PubMed Web of Science ®Google Scholar
• Triarhou L. C., Ghetti B. The dendritic dopamine projection of the substantia nigra: phenotypic denominator of weaver gene action in hetero- and homozygosity. Brain Res. 1989; 501: 373–381
   PubMedGoogle Scholar
• Vogelweid C. M., Verina T., Alyea C., Ghetti B. Pedominantly postmitotic degeneration of germ cells in the adult male weaver mutant mouse: a structural correlate of infertility. J. Neuropath. Exp. Neurol. 1993; 51: 333
   Google Scholar
• Vogelweid C. M., Verina T., Norton J., Harruff R., Ghetti B. Hypospermatogenesis is the cause of infertility in the male weaver mutant mouse. J. Neurogenetics 1993; 9: 89–104
   PubMed Web of Science ®Google Scholar
• Vogl A. W., Link R. W., Dym M. Colchicine-induced changes in the cytoskeleton of the golden-mantled ground squirrel (Spermophilus lateralis) Sertoli cells. Am. J. Anat. 1983; 168: 99–108
   PubMedGoogle Scholar