Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease

    Rachel Stewart, Megan C. King, Valerie Horsley
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    Studysummary This review discusses how the nuclear lamina integrates biochemical and mechanical signals to influence gene expression and skin homeostasis, but reports no new clinical results.
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    The document from 2018 examines the role of the nuclear lamina and the LINC complex in skin cell function and disease, particularly focusing on keratinocytes. It explains how the nuclear lamina, composed of A-type and B-type lamins, is involved in gene expression, genome integrity, and the integration of mechanical signals, which are essential for skin homeostasis and regeneration. The study highlights that lamin A/C disassembly and phosphorylation are crucial for keratinocyte differentiation, and mutations in lamin A can cause Hutchinson-Gilford Progeria Syndrome. The LINC complex is shown to be vital for transmitting mechanical stimuli to the nucleus, affecting nuclear proteome and mechanics, with implications for epidermal keratinocyte function and diseases like alopecia. The document also discusses the reorganization of chromatin during epidermal differentiation, the role of histone deacetylation, and chromatin remodelers in skin and hair follicle development. It suggests that the nuclear lamina and LINC complex respond to mechanical inputs, which may influence chromatin structure, gene expression, and differentiation, with further research needed to understand these mechanisms and their implications for skin diseases.
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