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MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway.


ABSTRACT: Skin development is governed by complex programs of gene activation and silencing, including microRNA-dependent modulation of gene expression. Here, we show that miR-214 regulates skin morphogenesis and hair follicle (HF) cycling by targeting ?-catenin, a key component of the Wnt signaling pathway. miR-214 exhibits differential expression patterns in the skin epithelium, and its inducible overexpression in keratinocytes inhibited proliferation, which resulted in formation of fewer HFs with decreased hair bulb size and thinner hair production. The inhibitory effects of miR-214 on HF development and cycling were associated with altered activities of multiple signaling pathways, including decreased expression of key Wnt signaling mediators ?-catenin and Lef-1, and were rescued by treatment with pharmacological Wnt activators. Finally, we identify ?-catenin as one of the conserved miR-214 targets in keratinocytes. These data provide an important foundation for further analyses of miR-214 as a key regulator of Wnt pathway activity and stem cell functions during normal tissue homeostasis, regeneration, and aging.

SUBMITTER: Ahmed MI 

PROVIDER: S-EPMC4242830 | biostudies-literature | 2014 Nov

REPOSITORIES: biostudies-literature

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MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway.

Ahmed Mohammed I MI   Alam Majid M   Emelianov Vladimir U VU   Poterlowicz Krzysztof K   Patel Ankit A   Sharov Andrey A AA   Mardaryev Andrei N AN   Botchkareva Natalia V NV  

The Journal of cell biology 20141101 4


Skin development is governed by complex programs of gene activation and silencing, including microRNA-dependent modulation of gene expression. Here, we show that miR-214 regulates skin morphogenesis and hair follicle (HF) cycling by targeting β-catenin, a key component of the Wnt signaling pathway. miR-214 exhibits differential expression patterns in the skin epithelium, and its inducible overexpression in keratinocytes inhibited proliferation, which resulted in formation of fewer HFs with decre  ...[more]

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