TY - JOUR
T1 - Regulation of the cytoskeleton in mesothelial cells
T2 - Reversible loss of keratin and increase in vimentin during rapid growth in culture
AU - Connell, Nancy D.
AU - Rheinwald, James G.
N1 - Funding Information:
We are grateful to Dr. Lee Parker and Mr. Neil Binder for frozen ampules of ascites fluid cells, and to Dr. Richard Hynes and Dr. Tung-Iien Sun for providing antisera. We thank Ms. Terry O’Connell and Ms. Susan Rehwoldt for their excellent technical assrstance, Ms. Lynne Dillon for her skillful preparation of the manuscript. Dr. Ying-Jy Wu for his valuable instruction on electrophoretic techniques, and Dr. Howard Green for his helpful comments on the manuscript. This research was supported by grants to J. G. R. from the National Institute on Aging and the National Cancer Institute.
PY - 1983/8
Y1 - 1983/8
N2 - Human mesothelial cells grew rapidly in culture when provided with serum, EGF, and hydrocortisone, adopting a fibroblastoid shape and forming parallel, multilayered arrays at saturation density. In the absence of EGF, the cells grew slowly to a flat, epithelioid monolayer similar to their normal pattern in vivo. Mesothelial cells normally have a high keratin and a low vimentin content in vivo. In culture, rapidly growing cells greatly reduced synthesis and content of their four major keratins to levels undetectable by immunofluorescence in most cells, but keratin synthesis and content returned to high levels whenever growth slowed. Vimentin synthesis and content was high during serial culture, but decreased several-fold in nondividing cells. The unique ability of the mesothelial cell to reversibly alter its morphology and intermediate filament composition is of unknown function and mechanism, but accounts for the morphological heterogeneity and the presence of keratin-negative cells in mesotheliomas.
AB - Human mesothelial cells grew rapidly in culture when provided with serum, EGF, and hydrocortisone, adopting a fibroblastoid shape and forming parallel, multilayered arrays at saturation density. In the absence of EGF, the cells grew slowly to a flat, epithelioid monolayer similar to their normal pattern in vivo. Mesothelial cells normally have a high keratin and a low vimentin content in vivo. In culture, rapidly growing cells greatly reduced synthesis and content of their four major keratins to levels undetectable by immunofluorescence in most cells, but keratin synthesis and content returned to high levels whenever growth slowed. Vimentin synthesis and content was high during serial culture, but decreased several-fold in nondividing cells. The unique ability of the mesothelial cell to reversibly alter its morphology and intermediate filament composition is of unknown function and mechanism, but accounts for the morphological heterogeneity and the presence of keratin-negative cells in mesotheliomas.
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U2 - 10.1016/0092-8674(83)90155-1
DO - 10.1016/0092-8674(83)90155-1
M3 - Article
C2 - 6192933
AN - SCOPUS:0020624204
SN - 0092-8674
VL - 34
SP - 245
EP - 253
JO - Cell
JF - Cell
IS - 1
ER -