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Spermatogenic cells of the prepuberal mouse: isolation and morphological characterization 总被引:62,自引:6,他引:56
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AR Bellve JC Cavicchia CF Millette DA O'Brien YM Bhatnagar M Dym 《The Journal of cell biology》1977,74(1):68-85
A procedure is described which permits the isolation from the prepuberal mouse testis of highly purified populations of primitive type A spermatogonia, type A spermatogonia, type B spermatogonia, preleptotene primary spermatocytes, leptotene and zygotene primary spermatocytes, pachytene primary spermatocytes and Sertoli cells. The successful isolation of these prepuberal cell types was accomplished by: (a) defining distinctive morphological characteristics of the cells, (b) determining the temporal appearance of spermatogenic cells during prepuberal development, (c) isolating purified seminiferous cords, after dissociation of the testis with collagenase, (d) separating the trypsin-dispersed seminiferous cells by sedimentation velocity at unit gravity, and (e) assessing the identity and purity of the isolated cell types by microscopy. The seminiferous epithelium from day 6 animals contains only primitive type A spermatogonia and Sertoli cells. Type A and type B spermatogonia are present by day 8. At day 10, meiotic prophase is initiated, with the germ cells reaching the early and late pachytene stages by 14 and 18, respectively. Secondary spermatocytes and haploid spermatids appear throughout this developmental period. The purity and optimum day for the recovery of specific cell types are as follows: day 6, Sertoli cells (purity>99 percent) and primitive type A spermatogonia (90 percent); day 8, type A spermatogonia (91 percent) and type B spermatogonia (76 percent); day 18, preleptotene spermatocytes (93 percent), leptotene/zygotene spermatocytes (52 percent), and pachytene spermatocytes (89 percent), leptotene/zygotene spermatocytes (52 percent), and pachytene spermatocytes (89 percent). 相似文献
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JU Nnadi IN Dimelu SI Nwani JC Madu CI Atama GN Attamah 《African Journal of Aquatic Science》2018,43(1):27-34
The current study investigated the effects of termite insecticide, Termex® (imidacloprid 35.50% SC), on biometric variations and oxidative stress biomarkers in Clarias gariepinus. Fish were exposed to 4.00 and 6.00 µg l–1 sublethal Termex® concentrations in 2017. The gill and liver tissues were sampled on days 7, 14, 21 and 28 and the results indicated that hepatosomatic index (HSI) decreased significantly when compared with the control on days 14, 21 and 28. The condition factor (CF) and viscera-somatic index (VSI) also decreased during the study period. The decrease was greater at 6.00 µg l–1 Termex® concentration on days 21 and 28 for CF and days 14 to 28 for VSI, respectively. The lipid peroxidation (LPO) in both tissues was highest in the 6.00 µg l?1 Termex® and increased with the duration. There was significant decrease (p < 0.05) in superoxide dismutase and glutathione peroxidase values, but significant increase in catalase activity in both tissues. The values of glutathione reductase in both tissues were comparable to the control, except on days 21 and 28 in the liver. There was negative correlation between the LPO in tissues and the HSI, CF and VSI values. The use of Termex® in the environment should be monitored to safeguard the health of aquatic organisms. 相似文献
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Phylogenetic utility of elongation factor-1 alpha in noctuoidea (Insecta: Lepidoptera): the limits of synonymous substitution 总被引:2,自引:1,他引:1
Mitchell A; Cho S; Regier JC; Mitter C; Poole RW; Matthews M 《Molecular biology and evolution》1997,14(4):381-390
To test its phylogenetic utility, nucleotide sequence variation in a
1,240-bp fragment of the elongation factor-1 alpha (EF-1 alpha) gene was
examined in 49 moth species representing the major groups of the
superfamily Noctuoidea. Both parsimony and distance analyses supported the
monophyly of nearly all groups for which there are clear morphological
synapomorphies. Clades of subfamily rank and lower, probably mid-Tertiary
and younger, were strongly supported. The third codon position contains 88%
of variable sites, and approaches saturation at approximately 20% sequence
divergence, possibly due to among-site rate heterogeneity and composition
bias; higher divergences occur only in association with shifts in
composition. Surprisingly, the few nonsynonymous changes appear no more
phylogenetically reliable than synonymous changes. Signal strength for
basal divergences is weak and fails to improve with character weighting;
thus, dense taxon sampling is probably needed for strong inference from
EF-1 alpha regarding deeper splits in Noctuoidea (probably early Tertiary).
EF-1 alpha synonymous changes show promise for phylogeny reconstruction
within Noctuidae and other groups of Tertiary age.
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