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流式细胞术测定睾丸和附睾中生精细胞DNA含量
引用本文:徐涛,李莉,闵志廉,朱有华.流式细胞术测定睾丸和附睾中生精细胞DNA含量[J].中华男科学杂志,2002,8(5):335-337.
作者姓名:徐涛  李莉  闵志廉  朱有华
作者单位:1. 解放军第88医院泌尿外科,山东,泰安,271000
2. 第二军医大学附属长征医院流式细胞室,上海,200003
3. 第二军医大学附属长征医院泌尿外科,上海,200003
摘    要:目的 :观察睾丸和附睾各段组织管腔内生精细胞DNA含量的变化。 方法 :利用流式细胞术 (FCM) ,对15例有生育能力、意外死亡的青年捐献者的右侧新鲜睾丸和附睾 (头、体、尾 )组织管腔内生精细胞的DNA含量进行测定。 结果 :从睾丸至附睾尾均存在单倍体 (1n)、二倍体 (2n)和四倍体 (4n) 3种细胞。 1n细胞由 (2 4 .87±7.2 8) %增至 (96 .33± 1.5 8) % ,其中睾丸至附睾每段之间的差异有极显著性 (P <0 .0 1) ,附睾体与附睾尾之间也有明显差别 (P <0 .0 5 )。 2n和 4n细胞的比例分别由 (6 3.0 7± 8.96 ) %、(9.4 3± 3.83) %下降至 (2 .4 7± 0 .93) %、(1.17± 0 .95 ) %。睾丸至附睾每段之间 2n细胞的比例差异有极显著性 (P <0 .0 1) ,附睾体与附睾尾之间也有明显差别(P <0 .0 5 ) ;除睾丸与附睾头之间的 4n细胞变化不明显外 (P >0 .0 5 ) ,其他各段之间的 4n细胞比例差异也有显著性 (P <0 .0 5 )。 结论 :未成熟生精细胞比例在附睾转运过程中逐渐减少

关 键 词:睾丸  附睾  生精细胞  DNA含量  流式细胞术  
文章编号:1009-3591(2002)05-0335-03
修稿时间:2001年11月5日

Analysis of DNA Content of Spermatogenic Cells in the Adult Human Testis and Epididymis by Flow Cytomety
Tao XU ,Li LI ,Zhi Lian MIN ,You Hua ZHU.Analysis of DNA Content of Spermatogenic Cells in the Adult Human Testis and Epididymis by Flow Cytomety[J].National Journal of Andrology,2002,8(5):335-337.
Authors:Tao XU  Li LI  Zhi Lian MIN  You Hua ZHU
Institution:Department of Urology, 88th Hospital of PLA, Tai'an, Shandong 271000, China.
Abstract:OBJECTIVES: To detect the changes of DNA ploidy of spermatogenic cells in testis and epididymis. METHODS: Right epididymides and testes from 15 fertile youth donors who died of accident were collected. Samples of spermatogenic cells in different regions of epididymis (caput, corpus and cauda) and tests were collected. DNA of spermatogenic cells were detected by flow cyctometry (FCM). RESULTS: The haploid(1n), diploid(2n) and tetraploid(4n) spermatogenic cells were existed in different regions of epididymis and testis. The 1n cells increased from (24.87 +/- 7.28)% in testis to (96.33 +/- 1.58)% in epididymis cauda, there were significant differences among regions of testis and epididymis caput, corpus(P < 0.01), and the difference among regions of epididymis corpus and epididymis cauda were also significant(P < 0.05). While the percentages of 2n and 4n cells decreased from (63.07 +/- 8.96)% and (9.43 +/- 3.83)% in tesits to (2.47 +/- 0.93)% and (1.17 +/- 0.95)% in epididymis respectively. There was significant difference of 2n cells between testis and epididymis caput, corpus(P < 0.01), and was also remarkable difference between epididymis corpus and cauda (P < 0.05). There was no difference of 4n cells between testis and epididymis caput(P > 0.05). There were significant difference among regions of epididymis caput, corpus and cauda(P < 0.05). CONCLUSIONS: The percentage of immature spermatogenic cells decreased along with passing through the epididymis.
Keywords:Testis  Epididymis  Spermatogenic cells  DNA content  Flow cytometry  Human
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