Winkelmann M, Pfitzer P, Schneider W
Abteilung Hämatologie, Onkologie und Klinische Immunologie, Universität Düsseldorf.
Klin Wochenschr. 1987 Dec 1;65(23):1115-31. doi: 10.1007/BF01734832.
Polyploidy--the doubling of chromosome sets of cells caused by a stop of mitosis at different levels of the mitotic cycle--is a phenomenon widely observed in plants, protozoa, metazoa, and animals. In man obligate polyploid tissues are found in liver parenchyma, heart muscle cells, and bone marrow megakaryocytes. Polyploidy occurs mostly in stable and highly differentiated cells and tissues. Besides age, stimulation of proliferation and increased metabolic function lead to polyploidization in these organs. Aneuploidy, however, is exclusively found in tumor cells. Megakaryocyte differentiation and polyploidy are controlled by thrombopoietin-like activities, of which the loci of production are still unknown. Megakaryocytes are unique among polyploid mammal cells. On the precursor level they maintain their proliferative activity independently of the mammal's age. Once having entered the incomplete mitotic cycle they stop cytokinesis and develop into highly polyploid cells. Polyploidization of megakaryocytes is the basic requirement for establishing highly effective hemostasis in mammals, which exhibit blood circulation based on high blood pressures. Every polyploidization results in increased production of membrane materials with which the platelet becomes endowed. By shedding cytoplasmic fragments approximately 3000 platelets are set free from a 32c megakaryocyte, compared with only 16 nucleated thrombocytes by mitotic division. There is further evidence that the heterogeneity of platelets mostly depends on the different polyploidy classes of the megakaryocytes from which they are derived. Changes in the polyploidy pattern of megakaryocytes could therefore have consequences for hemostatic disorders in several human diseases, particularly in malignancy.
多倍体——因有丝分裂周期不同阶段的有丝分裂停止导致细胞染色体组加倍——是在植物、原生动物、后生动物和动物中广泛观察到的一种现象。在人类中,肝脏实质、心肌细胞和骨髓巨核细胞中存在专性多倍体组织。多倍体大多发生在稳定且高度分化的细胞和组织中。除了年龄因素外,增殖刺激和代谢功能增强会导致这些器官发生多倍体化。然而,非整倍体仅在肿瘤细胞中发现。巨核细胞的分化和多倍体化受类血小板生成素活性控制,其产生位点尚不清楚。巨核细胞在多倍体哺乳动物细胞中是独特的。在前体水平,它们独立于哺乳动物的年龄维持其增殖活性。一旦进入不完全有丝分裂周期,它们就停止胞质分裂并发育成高度多倍体的细胞。巨核细胞的多倍体化是哺乳动物建立高效止血的基本要求,哺乳动物的血液循环基于高血压。每次多倍体化都会导致膜材料产量增加,血小板由此获得这些膜材料。通过脱落细胞质片段,一个32c的巨核细胞可释放约3000个血小板,而通过有丝分裂仅产生16个有核血小板。进一步的证据表明,血小板的异质性主要取决于它们所源自的巨核细胞的不同多倍体类别。因此,巨核细胞多倍体模式的变化可能会对几种人类疾病,尤其是恶性肿瘤中的止血障碍产生影响。