Dellagi K, Vainchenker W, Vinci G, Paulin D, Brouet J C
Laboratoire d'Immunologie et d'Immunopathologie, INSERM U. 108, Institut de Recherche sur les Maladies du Sang et Hĵpital Saint Louis, Paris, France.
EMBO J. 1983;2(9):1509-14. doi: 10.1002/j.1460-2075.1983.tb01615.x.
We describe the alterations of vimentin intermediate filament (IF) expression in human hemopoietic committed precursors as they differentiate into mature cells of the erythroid, granulomonocytic, megacaryocytic and lymphoid lineages. A double labelling fluorescence procedure was used to identify hemopoietic cells expressing lineage-specific antigens and to decorate the vimentin IF network. Whereas very early progenitors from each lineage expressed vimentin, the density and organization of the network differed strikingly as the cells matured on a given pathway. T lymphocytes, monocytes and granulocytes retained vimentin expression at all stages of maturation. In contrast, megakaryoblasts lose vimentin expression at a very early stage of differentiation, erythroblasts at variable steps between the committed erythroid cell and the red cell. Finally, B lymphocytes tend to lose vimentin expression later when they mature into plasma cells.
我们描述了人类造血定向祖细胞在分化为红系、粒单核系、巨核系和淋巴系成熟细胞过程中波形蛋白中间丝(IF)表达的变化。采用双重标记荧光法来鉴定表达谱系特异性抗原的造血细胞,并对波形蛋白IF网络进行染色。虽然每个谱系的极早期祖细胞都表达波形蛋白,但随着细胞在特定途径上成熟,网络的密度和组织差异显著。T淋巴细胞、单核细胞和粒细胞在成熟的各个阶段都保留波形蛋白表达。相比之下,巨核母细胞在分化的非常早期阶段就失去波形蛋白表达,成红细胞在定向红系细胞和红细胞之间的不同阶段失去表达。最后,B淋巴细胞在成熟为浆细胞时往往较晚失去波形蛋白表达。