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Biogeographic and disease-specific alterations in epidermal lipid composition and single-cell analysis of acral keratinocytes
Alexander A. Merleev, … , Johann E. Gudjonsson, Emanual Maverakis
Alexander A. Merleev, … , Johann E. Gudjonsson, Emanual Maverakis
Published July 28, 2022
Citation Information: JCI Insight. 2022;7(16):e159762. https://doi.org/10.1172/jci.insight.159762.
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Resource and Technical Advance Dermatology

Biogeographic and disease-specific alterations in epidermal lipid composition and single-cell analysis of acral keratinocytes

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Abstract

The epidermis is the outermost layer of skin. Here, we used targeted lipid profiling to characterize the biogeographic alterations of human epidermal lipids across 12 anatomically distinct body sites, and we used single-cell RNA-Seq to compare keratinocyte gene expression at acral and nonacral sites. We demonstrate that acral skin has low expression of EOS acyl-ceramides and the genes involved in their synthesis, as well as low expression of genes involved in filaggrin and keratin citrullination (PADI1 and PADI3) and corneodesmosome degradation, changes that are consistent with increased corneocyte retention. Several overarching principles governing epidermal lipid expression were also noted. For example, there was a strong negative correlation between the expression of 18-carbon and 22-carbon sphingoid base ceramides. Disease-specific alterations in epidermal lipid gene expression and their corresponding alterations to the epidermal lipidome were characterized. Lipid biomarkers with diagnostic utility for inflammatory and precancerous conditions were identified, and a 2-analyte diagnostic model of psoriasis was constructed using a step-forward algorithm. Finally, gene coexpression analysis revealed a strong connection between lipid and immune gene expression. This work highlights (a) mechanisms by which the epidermis is uniquely adapted for the specific environmental insults encountered at different body surfaces and (b) how inflammation-associated alterations in gene expression affect the epidermal lipidome.

Authors

Alexander A. Merleev, Stephanie T. Le, Claire Alexanian, Atrin Toussi, Yixuan Xie, Alina I. Marusina, Steven M. Watkins, Forum Patel, Allison C. Billi, Julie Wiedemann, Yoshihiro Izumiya, Ashish Kumar, Ranjitha Uppala, J. Michelle Kahlenberg, Fu-Tong Liu, Iannis E. Adamopoulos, Elizabeth A. Wang, Chelsea Ma, Michelle Y. Cheng, Halani Xiong, Amanda Kirane, Guillaume Luxardi, Bogi Andersen, Lam C. Tsoi, Carlito B. Lebrilla, Johann E. Gudjonsson, Emanual Maverakis

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Figure 4

Palmoplantar skin has a unique epidermal lipid composition.

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Palmoplantar skin has a unique epidermal lipid composition.
(A) Results ...
(A) Results are displayed as box-and-whisker plots, as described in Figure 1. Representative lipids were chosen to highlight the differences in lipid composition between PH (red arrow) and other anatomic locations. Note the low abundance of AS ceramide Cer(d16:1/28:0[2OH]) in PH skin and the increased abundance of AH ceramide Cer(t18:1[6OH]/22:0[2OH]). This pattern was also observed for all monitored ceramides with similar length sphingoid and fatty acid moieties (Supplemental Figure 2 and Supplemental Table 1). The acyl-ceramide EOSω-linoleoyloxy-Cer(d18:1/30:0) was also decreased in PH epidermis. (B) Additional examples of differentially expressed ceramides in PH skin that follow the same trends as presented in A. (C) Principal component analysis of lipid-associated metabolic gene expression data revealed complete separation of samples by anatomic location. (D) Whole-tissue RNA-Seq performed on palm and trunk biopsy specimens identifies differentially expressed lipid-associated metabolic genes. Genes presented here are relevant to the synthesis of the differentially expressed ceramides in PH epidermis presented in A and B.

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