- The last stage of barrier formation occurs within the extracellular spaces of the stratum corneum (SC), a sequence involving a family of lipid catabolic enzymes. Lamellar bodies (LB) deliver not only a mixture of nonpolar lipid, but also a family of lipid hydrolases to the SC interstices. Moreover, degradation of the plasma membrane makes an additional pool of lipid precursor, particularly sphingomyelin (SM), available for barrier formation. These enzymes are presumed to regulate the transformation of polar lipids (glucosylceramides, GlucCer; SM; phospholipids (PL); cholesterol sulfate, CS) to the three-component mixture of nonpolar lipids; i.e., ceramides (CER), free fatty acids (FFA), and cholesterol (CHOL), which form the lamellar unit structures required for barrier function in a terrestrial environment. Although considerable information is available about GlucCer-to-Cer processing, little is known about the regulation and requirement of PL-to-FFA, sphingomyelin SM-to-CER, and CS-to-CHOL processing. Moreover, the role of the SC pH gradient as an in situ regulator of lipid processing, and the sequential orchestration of lipid processing remains unexplored. Despite recent evidence that retinoid receptors regulate lipid processing transcriptionally, the target processing enzyme(s) is (are) not known. In this grant proposal; the investigators will assess: a) changes in lipid processing enzyme activity, content, mRNA, and localization in relation to barrier requirements; b) requirements for key processing steps in transgenic knockout mutant, and inhibitor-based models; c) the in situ regulation and orchestration of lipid processing; e) whether one or more lipid processing enzymes are regulated transcriptionally by retinoid receptors.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
2R01AR019098-22A1
Application #
2389336
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1979-04-01
Project End
2002-06-30
Budget Start
1997-08-01
Budget End
1998-06-30
Support Year
22
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Dermatology
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Hu, Lizhi; Mauro, Theodora M; Dang, Erle et al. (2017) Epidermal Dysfunction Leads to an Age-Associated Increase in Levels of Serum Inflammatory Cytokines. J Invest Dermatol 137:1277-1285
Man, George; Mauro, Theodora M; Zhai, Yongjiao et al. (2015) Topical hesperidin enhances epidermal function in an aged murine model. J Invest Dermatol 135:1184-1187
Elias, Peter M (2015) Stratum corneum acidification: how and why? Exp Dermatol 24:179-80
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Ye, Li; Lv, Chengzhi; Man, George et al. (2014) Abnormal epidermal barrier recovery in uninvolved skin supports the notion of an epidermal pathogenesis of psoriasis. J Invest Dermatol 134:2843-2846
Elias, Peter M (2014) Lipid abnormalities and lipid-based repair strategies in atopic dermatitis. Biochim Biophys Acta 1841:323-30
Xin, Shujun; Mauro, Jacqueline A; Mauro, Theodora M et al. (2014) Ten-year publication trends in dermatology in mainland China. Int J Dermatol 53:e438-42
Man, George; Mauro, Theodora M; Kim, Peggy L et al. (2014) Topical hesperidin prevents glucocorticoid-induced abnormalities in epidermal barrier function in murine skin. Exp Dermatol 23:645-51
Man, Mao-Qiang; Lin, Tzu-Kai; Santiago, Juan L et al. (2014) Basis for enhanced barrier function of pigmented skin. J Invest Dermatol 134:2399-2407
Elias, Peter M; Gruber, Robert; Crumrine, Debra et al. (2014) Formation and functions of the corneocyte lipid envelope (CLE). Biochim Biophys Acta 1841:314-8

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