Skin pharmacology and physiology · 2021
[Pathogenic and Compensatory Mechanisms in Epidermis of Sphingomyelin Synthase 2-Deficient Mice].
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
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
Аннотация
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 (SC). 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 non-lethal gene abnormality can cause an ichthyotic skin phenotype.