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Right, immunofluorescent staining for the T cell marker CD3 (green) in control and Rag1 KO skin (n = 6 mice for each condition, two-tailed unpaired t-test). E.M.F. 138, 172–176 (2003). A., Kaur, G., Sausville, E. A. J. 88881.162285/2017-01) and is supported by a FAPESP grant (2013/08216-2); E.M.F. Mechanisms, hallmarks, and implications of stem cell quiescence. Peters, E. M. J., Tobin, D. J., Botchkareva, N., Maurer, M. & Paus, R. Migration of melanoblasts into the developing murine hair follicle is accompanied by transient c-Kit expression. Source data, a, Left, immunofluorescent staining of hair follicles for phosphorylated CREB (pCREB; green) and TRP2 (red) 12 h after RTX injection.
h, Left, schematic of the strategy for isolation of MeSCs.
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i, Quantification of the number of MeSCs in the skin of mice injected with saline or RTX. We use cookies to help provide and enhance our service and tailor content and ads.
Nat. Source data, a, Left, immunofluorescent staining of active caspase-3 (aCAS3; green) and TRP2 (red) from mice one day after injection with RTX or noradrenaline. Cite as. Source data for all main figures and Extended Data figures are provided with the paper. NFIB is a governor of epithelial-melanocyte stem cell behaviour in a shared niche. Marshall, I. C. B. et al. Proc Natl Acad Sci U S A 114(34):E7101–E7110, Eisinger M, Marko O (1982) Selective proliferation of normal human melanocytes in vitro in the presence of phorbol ester and cholera toxin.
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