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小鼠生精细胞增殖与凋亡的年龄变化
引用本文:张健,高福禄,支会英,段相林.小鼠生精细胞增殖与凋亡的年龄变化[J].动物学报,2001,47(2):209-214,T001,T002.
作者姓名:张健  高福禄  支会英  段相林
作者单位:1. 河北师范大学生命科学学院,
2. 河北承德医学院组胚教研室,
3. 河北医科大学生化教研室,
基金项目:河北省自然科学基金,河北师范大学校科研和教改项目,300164,,,
摘    要:为研究雄性小鼠睾丸在发生,发育过程生精细胞增殖与凋亡的年龄变化,本研究采用了免疫细胞化学,凋亡细胞原位检测,电镜及体视学图象分析等方法,对胚胎15天到生后10月后发育阶段生精细胞的超微结构,PCNA表达,凋亡情况进行了较深入地研究,结果:(1)精原细胞PCNA反应在胚胎15天为阳性,从胚胎18天到生后5天,降为弱阳性,而阳性的精原细胞在生后7天重新出现,一直到生后6月,仍可见部分精原细胞呈阳性反应;(2)生后3天,可见凋亡的精原细胞染色质浓缩,核膜出现明显的核周隙,核碎裂,凋亡细胞数从生后1天到生后第3周有增加的趋势,于生后第3周出现峰值,之后降低,之后降低,结论:(1)PCNA阳性细胞而密度到生后第2周出现峰值,而凋亡细胞数于生后3周出现峰值,生精细胞凋亡的高峰要滞后其增殖峰1周左右,而且与其所处生精周期的特定阶段有关;(2)精原细胞在胚胎发育过程中向曲细精管周边迁移,其排列由无序到有序;(3)在生后各发育 ,精原细胞始终保持DNA复制的能力。

关 键 词:小鼠  生精细胞  增殖  年龄变化  细胞凋亡

AGE-SPECIFIC CHANGES OF PROLIFERATION AND APOPTOSIS IN THE SEMINIFEROUS EPITHELIUM OF LABORATORY MICE
ZHANG Jian,GAO Fu-lu,ZHI Hui-Ying,DUAN Xiang-lin.AGE-SPECIFIC CHANGES OF PROLIFERATION AND APOPTOSIS IN THE SEMINIFEROUS EPITHELIUM OF LABORATORY MICE[J].Acta Zoologica Sinica,2001,47(2):209-214,T001,T002.
Authors:ZHANG Jian  GAO Fu-lu  ZHI Hui-Ying  DUAN Xiang-lin
Abstract:The ultrastructure, cell apoptosis and proliferation of the spermatogenic ce lls in mice during a series of development stages from 15th day of fetus to 10th month a fter birth were observed with a variety of techniques,such as immunocytochemist ry (ICC), TUNEL method for detection of apoptotic cells in situ,electron mi cros copy and analysis of morphometry. The results demonstrated~that:(1)The PCNA positive s permatogonium were found at 15th day of fetus,then decreased from 18th day of fetus to the 5th day postnatal. At postnatal 7th day,the PCNA positive spermatogo nium were found again,at the same time ,the spermatogonium were partly found p ositive till 6th month after birth; (2)At 3rd day after birth,the pyknotic chro matin in nucleus and progressive degeneration in plasmic structures were observe d. The number of apoptotic cells reached its peaks on postnatal 21st day. Conclu sion:(1)Surface densities of PCNA positive cells reached their peaks on 14th day after birth,but the number of apoptotic cells reached its peaks on 21st day p ostnatal,so the apoptotic peak was late the proliferating peak for a week,and related to the particular period in cycle of seminiferous epithelium; (2)The spe rmatogium were found move from center to the periphery of the seminiferous tubule and arrange disorder to order;(3)The spermatogonium remained replicating activ ity of DNA during the developing stage.
Keywords:Mouse      Spermatogenic cell    Proliferation      Apoptosis    Age  specific change
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