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巨核细胞生成是否存在自身调节?

Does autoregulation of megakaryocytopoiesis occur?

作者信息

Ebbe S, Phalen E

出版信息

Blood Cells. 1979 Mar 23;5(1):123-38.

PMID:555684
Abstract

Although a major regulator of thrombocytopoiesis is the number of circulating platelets, several observations suggest that independent alternative regulatory mechanisms may exist. In some situations there is a curious association of megakaryocytopenia and megakarocytic macrocytosis in spite of normal platelet counts. If macrocytosis is considered as a sign of stimulation, this association suggests a cause and effect relationship between decreased numbers and increased size of megakaryocytes. This thesis was tested by examining the delayed effects of sublethal irradiation and the acute effects of hydroxyurea in mice. It was found that megakaryocytopenia and macromegakaryocytosis occurred together and that platelets counts were either normal or only slightly reduced. Therefore it was concluded that normal numbers of platelets could be produced by decreased numbers of megakaryocytes. Megakaryocytopenia appeared to be compensated, in part, by increased size of megakaryocytes, but the mechanism by which this occurred has not been elucidated. It is postulated that a reduction in the number of cells of the megakaryocytic system is sensed by a homeostatic mechanism that then acts to stimulate the cells that are present. This stimulation may then be manifested as macrocytosis of megakaryocytes.

摘要

虽然血小板生成的一个主要调节因素是循环血小板的数量,但一些观察结果表明可能存在独立的替代调节机制。在某些情况下,尽管血小板计数正常,但却存在巨核细胞减少症与巨核细胞性大细胞症的奇特关联。如果将大细胞症视为刺激的标志,那么这种关联表明巨核细胞数量减少与大小增加之间存在因果关系。通过研究亚致死剂量照射的延迟效应和羟基脲对小鼠的急性效应来验证这一论点。结果发现,巨核细胞减少症和巨核细胞增多症同时出现,并且血小板计数要么正常,要么仅略有降低。因此得出结论,巨核细胞数量减少也可以产生正常数量的血小板。巨核细胞减少症似乎部分地通过巨核细胞大小增加得到补偿,但其发生机制尚未阐明。据推测,巨核细胞系统细胞数量的减少被一种稳态机制感知,该机制随后作用于刺激现存的细胞。这种刺激随后可能表现为巨核细胞的大细胞症。

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