Sathananthan A H
Faculty of Health Sciences, La Trobe University, Melbourne, Australia.
Histol Histopathol. 1997 Jul;12(3):827-56.
The pattern of sperm centrosomal (centriolar) inheritance, centrosomal replication and perpetuation during mitosis of the human embryo is reviewed with a series of electron micrographs. Embryonic cleavage involves repeated mitoses, a convenient sequence to study centriolar behaviour during cell division. After the paternal inheritance of centrioles in the human was reported (Sathananthan et al., 1991a), there has been an upsurge of centrosomal research in mammals, which largely follow the human pattern. The human egg has an inactive non-functional centrosome. The paternal centrosome contains a prominent centriole (proximal) associated with pericentriolar material which is transmitted to the embryo at fertilization and persists during sperm incorporation. Centriolar duplication occurs at the pronuclear stage (interphase) and the centrosome initially organizes a sperm aster when male and female pronuclei breakdown (prometaphase). The astral centrosome containing diplosomes (two typical centrioles) splits and relocates at opposite poles of a bipolar spindle to establish bipolarization, a prerequisite to normal cell division. Single or double centrioles occupy pivotal positions on spindle poles and paternal and maternal chromosomes organize on the equator of a metaphase spindle, at syngamy. Bipolarization occurs in all monospermic and in most dispermic ova. Dispermic embryos occasionally form two sperm asters initially and produce tripolar spindles (tripolarization). Anaphase and telophase follows producing two or three cells respectively, completing the first cell cycle. Descendants of the sperm centriole were found at every stage of perimplantation embryo development and were traced from fertilization through cleavage (first four cell cycles) to the morula and hatching blastocyst stage. Centrioles were associated with nuclei at interphase, when they were often replicating and occupied pivotal positions on spindle poles during mitosis. Sperm remnants were associated with centrioles and were found at most stages of cleavage. Centrioles were found in trophoblast, embryoblast and endoderm cells in hatching blastocysts. Pericentriolar, centrosomal material nucleated astral and spindle microtubules. Abnormal nuclear configurations observed in embryos reflect mitotic aberrations. The bovine embryo closely resembles the human embryo in centriolar behaviour during mitosis. It is concluded that the sperm centrosome is the functional active centrosome in humans and is likely the ancestor of centrioles within centrosomes in foetal and adult somatic cells. The role of the sperm centrosome in embryogenesis and male infertility is discussed, since it is of clinical importance in assisted reproduction.
本文通过一系列电子显微镜照片,综述了人类胚胎有丝分裂过程中精子中心体(中心粒)的遗传模式、中心体复制及延续情况。胚胎卵裂涉及反复的有丝分裂,这是研究细胞分裂过程中中心粒行为的便利序列。在报道了人类中中心粒的父系遗传(Sathananthan等人,1991a)之后,哺乳动物的中心体研究激增,且大多遵循人类模式。人类卵子有一个无活性、无功能的中心体。父系中心体包含一个与中心粒周围物质相关的显著中心粒(近端),该物质在受精时传递给胚胎,并在精子融合过程中持续存在。中心粒复制发生在原核期(间期),当雄原核和雌原核解体时(前中期),中心体最初组织形成一个精子星体。含有双联体(两个典型中心粒)的星体中心体分裂并重新定位到双极纺锤体的相对两极以建立双极化,这是正常细胞分裂的前提条件。在受精时,单个或双个中心粒在纺锤体极上占据关键位置,父系和母系染色体在中期纺锤体的赤道面上排列。双极化发生在所有单精受精和大多数双精受精的卵子中。双精受精的胚胎偶尔最初会形成两个精子星体并产生三极纺锤体(三极化)。随后进入后期和末期,分别产生两个或三个细胞,完成第一个细胞周期。在植入前胚胎发育的每个阶段都发现了精子中心粒的后代,并追踪其从受精到卵裂(前四个细胞周期)直至桑椹胚和孵化囊胚阶段。在间期,中心粒与细胞核相关联,此时它们常进行复制,在有丝分裂期间在纺锤体极上占据关键位置。精子残余物与中心粒相关联,在卵裂的大多数阶段都能发现。在孵化囊胚的滋养层、胚泡内细胞团和内胚层细胞中发现了中心粒。中心粒周围的中心体物质形成星体和纺锤体微管的核。胚胎中观察到的异常核形态反映了有丝分裂异常。牛胚胎在有丝分裂过程中的中心粒行为与人类胚胎非常相似。得出的结论是,精子中心体是人类中具有功能活性的中心体,很可能是胎儿和成年体细胞中心体内中心粒的祖先。鉴于精子中心体在辅助生殖中具有临床重要性,本文还讨论了其在胚胎发生和男性不育中的作用。