LACK OF LAMIN-A AND LAMIN-C IN MAMMALIAN HEMATOPOIETIC-CELL LINES DEVOID OF INTERMEDIATE FILAMENT PROTEINS
- 1 October 1988
- journal article
- research article
- Vol. 47 (1) , 121-131
Abstract
Using immunofluorescence microscopy and immunoblot analysis, we have examined the composition of the nuclear lamina in several murine and human cell lines. Whereas it was shown that intermediate filament-positive Ehrlich ascites tumor and HeLa-S3 cells contain the three major mammalian lamin subspecies, only lamin B could be detected in several myeloid- and lymphoid-derived cell lines representative of distinct stages in hemopoietic differentiation but all devoid of cytoplasmic intermediate filament proteins. These included the murine plasmacytoma cell types MPC-11 and MOPC-31C, murine myeloma cells X63-Ag8.6.5.3 and human promyelocytic leukemia cells HL-60. Our results provide the first evidence that mammalian somatic cells capable of normal proliferation may lack both cytoplasmic intermediate filament proteins and a normal complement of nuclear lamins.This publication has 8 references indexed in Scilit:
- Change of karyoskeleton during spermatogenesis of Xenopus: expression of lamin LIV, a nuclear lamina protein specific for the male germ line.Proceedings of the National Academy of Sciences, 1985
- Changes in the nuclear lamina composition during early development of Xenopus laevisCell, 1985
- Changes in distribution of nuclear matrix antigens during the mitotic cell cycle.The Journal of cell biology, 1984
- The redistribution of a conserved nuclear envelope protein during the cell cycle suggests a pathway for chromosome condensationCell, 1984
- Intermediate filament protein synthesis in preimplantation murine embryosDevelopmental Biology, 1983
- A monoclonal antibody which recognises each of the nuclear lamin polypeptides in mammalian cells.The EMBO Journal, 1983
- Reorganization of arrays of prekeratin filaments during mitosisExperimental Cell Research, 1981
- Monoclonal antibodies against trophectoderm-specific markers during mouse blastocyst formation.Proceedings of the National Academy of Sciences, 1980