Expression of the nuclear membrane protein statin in cycling cells
- 1 April 1993
- journal article
- research article
- Published by Wiley in The Journal of Pathology
- Vol. 169 (4) , 391-396
- https://doi.org/10.1002/path.1711690402
Abstract
Statin is a 57 kD protein previously reported to be expressed by cells in G0. We have studied the detailed distribution of statin immunoreactivity in normal human and rat tissues, and correlated this with investigation of in vitro model systems. By laser confocal microscopy, statin immunoreactivity is localized to the nuclear membrane. In contrast to previous reports, using in vitro model systems we found that statin was also expressed by replicating cells as judged by both co-localization with [3H]thymidine-labelled and Ki67-labelled cells. Furthermore, in a nude mouse xenograft model the number of statin-labelled cells exceeded the number of quiescent cells as assessed by both fraction of labelled mitosis methods and labelling with [3H]thymidine and Ki67. We conclude that although there is an association between expression of the 57 kD nuclear membrane protein statin and growth arrest, this is not absolute and it is expressed in a sub-population of cycling cells. The properties of statin closely resemble those of nuclear lamins, members of the intermediate filament family.Keywords
This publication has 17 references indexed in Scilit:
- A comparison of immunohistochemical markers of cell proliferation with experimentally determined growth fractionThe Journal of Pathology, 1991
- From growth arrest to growth suppressionJournal of Cellular Biochemistry, 1991
- The relationship of expression of statin, the nuclear protein of nonproliferating cells, to the differentiation and cell cycle of astroglia in cultures and in situJournal of Neuroscience Research, 1990
- Characterization of two populations of statin and the relationship of their syntheses to the state of cell proliferation.The Journal of cell biology, 1990
- The disappearance of a cyclin-like protein and the appearance of statin is correlated with the onset of differentiation during myogenesis in vitroExperimental Cell Research, 1988
- Contact‐inhibition‐induced quiescent state is marked by intense nuclear expression of StatinJournal of Cellular Physiology, 1987
- Measurement of the Rate of Epidermal Terminal Differentiation: Expression of Involucrin by S-Phase Keratinocytes in Culture and in Psoriatic PlaquesJournal of Investigative Dermatology, 1987
- Disapparence of statin, a protein marker for non-proliferating and senescent cells, following serum-stimulated cell cycle entryExperimental Cell Research, 1986
- Rapid disappearance of statin, a nonproliferating and senescent cell-specific protein, upon reentering the process of cell cycling.The Journal of cell biology, 1985
- A 57,000-mol-wt protein uniquely present in nonproliferating cells and senescent human fibroblasts.The Journal of cell biology, 1985