| Literature DB >> 33915532 |
Shota Sakai1,2, Asami Makino3, Akihito Nishi4, Takeshi Ichikawa5, Tadashi Yamashita4, Makoto Taniguchi5, Yoshihiro Tokudome6, Yoshio Hirabayashi7, Masashi Akiyama6, Debra Crumrine8,9, Yoshikazu Uchida8,9, Peter M Elias8,9, Tetsuya Tsuchida10, Sumiko Hamanaka10.
Abstract
Sphingomyelin (SM) is a constituent of cellular membranes, while ceramides (Cer) produced from SM on plasma membranes serve as a lipid mediator that regulates cell proliferation, differentiation, and apoptosis. In the skin, SM also is a precursor of Cer, an important constituent of epidermal permeability barrier. We investigated the role of epidermal SM synthase (SMS)2, an isoform of SMS, which modulates SM and Cer levels on plasma membranes. Although SMS2-knockout (SMS2-KO) mice were not neonatal lethal, an ichthyotic phenotype with epidermal hyperplasia and hyperkeratosis was evident at birth, which persisted until 2 weeks of age. These mice showed abnormal lamellar body morphology and secretion, and abnormal extracellular lamellar membranes in the stratum corneum. These abnormalities were no longer evident by 4 weeks of age in SMS2-KO mice. Our study suggests that (1) exposure to a dry terrestrial environment initiates compensatory responses, thereby normalizing epidermal ichthyotic abnormalities and (2) that a nonlethal gene abnormality can cause an ichthyotic skin phenotype.Entities:
Keywords: Differentiation; Keratinocyte; Proliferation; Skin barrier function; Sphingomyelin; Sphingomyelin synthase
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Year: 2021 PMID: 33915532 PMCID: PMC8410625 DOI: 10.1159/000515608
Source DB: PubMed Journal: Skin Pharmacol Physiol ISSN: 1660-5527 Impact factor: 3.479