Metcalf D
Nouv Rev Fr Hematol (1978). 1978;20(4):521-33.
The development of in vitro cloning systems for populations of hemopoietic and lymphoid cells has enabled a family of specific regulatory macromolecules to be detected and characterized. These macromolecules control proliferation and differentiation in hemopoietic cell populations. Studies have demonstrated the complexity of the spectrum of molecules which are involved in the regulation of each group of hemopoietic cells. Heterogeneous subpopulations of molecules exist for each regulatory function and more than one molecular form exists for the various regulator molecules. While the cellular origin of many of these regulators has not been clearly demonstrated, it is apparent that hemopoietic populations themselves can be significant sources of both stimulatory and inhibitory regulators. In particular, there are now clear examples of regulatory interactions which occur in both directions between hemopoietic and lymphoid populations. While in no case a complete analysis of the control systems has been achieved, maintenance of homeostasis in hemopoietic systems is now better understood than for most other cell populations in the body. Further, with existing techniques, and in particular, the exploitation of the full potential of the semi-solid cloning systems, it is realistic to expect that a complete analysis of hemopoietic regulation can now be accomplished.
造血细胞和淋巴细胞群体体外克隆系统的发展,使得一类特定的调节性大分子得以被检测和鉴定。这些大分子控制着造血细胞群体的增殖和分化。研究表明,参与每组造血细胞调节的分子谱非常复杂。每种调节功能都存在分子的异质性亚群,各种调节分子也存在不止一种分子形式。虽然其中许多调节因子的细胞来源尚未得到明确证实,但显然造血细胞群体本身可以是刺激和抑制调节因子的重要来源。特别是,现在有明确的例子表明造血和淋巴细胞群体之间存在双向调节相互作用。虽然尚未对控制系统进行全面分析,但目前对造血系统中稳态维持的理解比对体内大多数其他细胞群体更好。此外,利用现有技术,特别是充分发挥半固体克隆系统的潜力,现在有望完成对造血调节的全面分析。