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Journal of Cell Science, Vol 93, Issue 3 409-418, Copyright © 1989 by Company of Biologists
JOURNAL ARTICLES |
M Philpott, MR Green and T Kealey
Nuffield Department of Clinical Biochemistry, University of Oxford, John Radcliffe Hospital, Headington, UK.
We have already shown that shearing can be used to yield large numbers of viable intact hair follicles. We now show that these follicles can be viably maintained on permeable supports for 7 days in vitro as determined by their adenine nucleotide contents, rates of [methyl-3H]thymidine and [U-14C]leucine uptake, [methyl-3H]thymidine autoradiography, patterns of keratin synthesis and light and electron microscopy. These studies, however, show that after 7 days maintenance the morphology of maintained follicles shows a closer resemblance to the telogen rather than the anagen follicle. We therefore conclude that the failure of previous attempts at maintaining hair growth in culture is due to hair follicles prematurely entering the resting stage of their hair growth cycle, possibly as a response to isolation.