Johnson L
Department of Veterinary Anatomy and Public Health, College of Veterinary Medicine, Texas A&M University, College Station 77843-4458, USA.
Microsc Res Tech. 1995 Dec 1;32(5):385-422. doi: 10.1002/jemt.1070320504.
Spermatogenesis is a process of division and differentiation by which spermatozoa are produced in seminiferous tubules. A measure of efficiency of spermatogenesis is the estimated number of spermatozoa produced per day per gram of testicular parenchyma. This measure is not influenced by species differences in testicular size; however, it is influenced by species differences in the numerical density of germ cells and in the life spans of these cells. Seminiferous tubules are composed of somatic cells (myoid cells and Sertoli cells), and germ cells (spermatogonia, spermatocytes, and spermatids). Activity of these three germ cells divide spermatogenesis into spermatocytogenesis, meiosis, and spermiogenesis, respectively. Spermatocytegenesis involves mitotic cell division to increase the yield of spermatogenesis and to produce stem cells and primary spermatocytes. Meiosis involves duplication and exchange of genetic material and two cell divisions that reduce the chromosome number and yield four spermatids. Spermiogenesis is the differentiation of spherical spermatids into mature spermatids which are released at the luminal free surface as spermatozoa. The spermatogenic cycle is superimposed on the three major divisions of spermatogenesis. Spermatogenesis and germ cell degeneration can be quantified from numbers of germ cells in various steps of development throughout spermatogenesis, and quantitative measures are related to number of spermatozoa in the ejaculate. Germ cell degeneration occurs throughout spermatogenesis; however, the greatest impact occurs during spermatocytogenesis and meiosis. Efficiency of spermatogenesis is related to the amount of germ cell degeneration, pubertal development, season of the year, and aging of humans and animals. Number of Sertoli cells and amount of smooth endoplasmic reticulum of Leydig cells (but not Leydig cell number) are related to efficiency of spermatogenesis. In humans, efficiency of spermatogenesis is reflected in number of spermatogenic stages per cross-section and number of missing generations within each stage; however, the arrangement of stages along the tubular length does not reflect differences in the efficiency of spermatogenesis. In short, spermatogenesis involves both mitotic and meiotic cell divisions and an unsurpassed example of cell differentiation in the production of the spermatozoon, and daily sperm production per g parenchyma is a measure of its efficiency.
精子发生是一个分裂和分化的过程,通过这个过程,生精小管中产生精子。精子发生效率的一个衡量标准是每克睾丸实质每天产生的精子估计数量。这个衡量标准不受睾丸大小的物种差异影响;然而,它受生殖细胞数量密度和这些细胞寿命的物种差异影响。生精小管由体细胞(肌样细胞和支持细胞)和生殖细胞(精原细胞、精母细胞和精子细胞)组成。这三种生殖细胞的活动分别将精子发生分为精母细胞发生、减数分裂和精子形成。精母细胞发生涉及有丝分裂细胞分裂,以增加精子发生的产量并产生干细胞和初级精母细胞。减数分裂涉及遗传物质的复制和交换以及两次细胞分裂,这些分裂减少染色体数量并产生四个精子细胞。精子形成是球形精子细胞分化为成熟精子细胞的过程,成熟精子细胞作为精子在管腔游离表面释放。精子发生周期叠加在精子发生的三个主要阶段之上。精子发生和生殖细胞退化可以通过整个精子发生过程中不同发育阶段的生殖细胞数量来量化,并且定量测量与射精中的精子数量相关。生殖细胞退化在整个精子发生过程中都会发生;然而,最大的影响发生在精母细胞发生和减数分裂期间。精子发生效率与生殖细胞退化的程度、青春期发育、一年中的季节以及人类和动物的衰老有关。支持细胞的数量和睾丸间质细胞的滑面内质网的数量(但不是睾丸间质细胞的数量)与精子发生效率有关。在人类中,精子发生效率反映在每个横截面上的生精阶段数量以及每个阶段内缺失的世代数量;然而,沿管长的阶段排列并不能反映精子发生效率的差异。简而言之,精子发生涉及有丝分裂和减数分裂细胞分裂,并且是精子产生过程中细胞分化的一个无与伦比的例子,每克实质的每日精子产量是其效率的一个衡量标准。