Mitosis in the human embryo: the vital role of the sperm centrosome (centriole)

A.H. Sathananthan

Faculty of Health Sciences, La Trobe University, Melbourne, Australia, Institute of Reproduction and Development, Monash Medical Centre, Melbourne, Australia and Department of Obstetrics and Gynaecology, National University Hospital, Singapore

Offprint requests to: Dr. A.H. Sathananthan, Associate Professor/Reader, Faculty of Health Sciences. La Trobe University, Bundoora, Victoria 3083. Australia

Summary. The pattern of sperm centrosomal (centriolar) inheritance, centrosomal rep lication 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 matern al chromosomes organize on the equator of a metaphase spindle, at syngamy. Bipolarization occurs in all monospermic and in most dispermicova. Dispermic embryos occasionally form two sperm asters initially and produce tripolar spindles ( tripolarization). Anaphase and te lophase follows producing two or three cells respectively, completing the first cell cycle. Descendants of the sperm centriole were found at every stage of preimplantation 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 fo und 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. Histol Histopathol 12, 827-856 (1997)

Key words: Sperm centriole, Fertilization, Human embyro, Mitosis, Ultrastructure

DOI: 10.14670/HH-12.827