日本語フィールド
著者：Sakai, Shota; Makino, Asami; Nishi, Akihito; Ichikawa, Takeshi; Yamashita, Tadashi; Taniguchi, Makoto; Tokudome, Yoshihiro; Hirabayashi, Yoshio; Akiyama, Masashi; Crumrine, Debra; Uchida, Yoshikazu; Elias, Peter M.; Tsuchida, Tetsuya; Hamanaka, Sumiko題名：Pathogenic and Compensatory Mechanisms in Epidermis of Sphingomyelin Synthase 2-Deficient Mice発表情報：Skin Pharmacology and Physiology 巻: 34 号: 5 ページ: 246 - 252キーワード：概要：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.抄録：英語フィールド
Author：Sakai, Shota; Makino, Asami; Nishi, Akihito; Ichikawa, Takeshi; Yamashita, Tadashi; Taniguchi, Makoto; Tokudome, Yoshihiro; Hirabayashi, Yoshio; Akiyama, Masashi; Crumrine, Debra; Uchida, Yoshikazu; Elias, Peter M.; Tsuchida, Tetsuya; Hamanaka, SumikoTitle：Pathogenic and Compensatory Mechanisms in Epidermis of Sphingomyelin Synthase 2-Deficient MiceAnnouncement information:Skin Pharmacology and Physiology Vol: 34 Issue: 5 Page: 246 - 252An 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.