Evidence map›Paper›PMID 42905353›Full record

ArticleGenes & genomics2026

Transcriptomic profiling suggests restoration of epidermal barrier-associated lipid metabolism in Egr1-deficient skin following house dust mite exposure.

Euitaek Jung, Yena Choi, HeeWon Kang, Soon Young Shin

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Article in Genes & genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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4 authors.

Euitaek Jung *Department of Biological Sciences, College of Life Science, Konkuk University, Seoul, 05029, Republic of Korea.ORCID http://orcid.org/0000-0003-3091-0649
Yena Choi *Department of Biological Sciences, College of Life Science, Konkuk University, Seoul, 05029, Republic of Korea.ORCID http://orcid.org/0009-0007-2547-5458
HeeWon KangDepartment of Biological Sciences, College of Life Science, Konkuk University, Seoul, 05029, Republic of Korea.ORCID http://orcid.org/0009-0000-2377-658X
Soon Young ShinDepartment of Biological Sciences, College of Life Science, Konkuk University, Seoul, 05029, Republic of Korea. shinsy@konkuk.ac.kr.ORCID http://orcid.org/0000-0002-1075-0011

Funding

Korea Drug Development Fund HN21C0984National Research Foundation of Korea 2023R1A2C1003601
6 · The paper itself

Abstract

backgroundHouse dust mite (HDM) is a major environmental allergen that promotes cutaneous inflammation and disrupts epidermal barrier-associated processes. Early growth response 1 (EGR1) is an inducible transcription factor implicated in inflammatory skin responses; however, its relationship with epidermal barrier-associated lipid metabolism during allergen exposure remains poorly understood.

objectiveThis study investigated whether Egr1 deficiency is associated with preservation of epidermal barrier-related features and restoration of lipid metabolic transcriptional programs following HDM exposure.

methodsEpidermal alterations and filaggrin (FLG) expression were evaluated in wild-type (WT) and Egr1-knockout (KO) mice following topical HDM exposure. A previously generated RNA-seq dataset from WT and Egr1-KO skin with or without HDM treatment was reanalyzed as an exploratory transcriptomic dataset. Expression-change profiling, functional enrichment, and gene set enrichment analyses were used to identify HDM-responsive transcriptional patterns associated with Egr1 deficiency. Selected lipid metabolism-associated genes were independently examined by quantitative real-time PCR.

resultsHDM exposure induced epidermal abnormalities and markedly reduced FLG expression in WT mice, whereas these changes were attenuated in Egr1-KO mice. Exploratory transcriptomic profiling suggested that Egr1 deficiency reprogrammed, rather than globally suppressed, the transcriptional response to HDM. Genes suppressed by HDM but restored in Egr1-deficient skin were preferentially associated with lipid metabolic processes, including fatty acid and sphingolipid metabolism. Gene set enrichment analysis further showed reciprocal enrichment of several lipid-related pathways between WT-HDM versus WT-control and KO-HDM versus WT-HDM comparisons. Independent expression analysis supported the recovery of Elovl6, Hacd2, and Cidec in HDM-treated Egr1-KO skin.

conclusionEgr1 deficiency is associated with attenuation of HDM-induced FLG loss and restoration of selected epidermal lipid metabolism-associated transcriptional patterns. These findings suggest that EGR1-associated inflammatory responses may intersect with epidermal lipid metabolism during allergen exposure and provide a basis for further investigation of EGR1 in the inflammation-barrier interface.

Indexed as

Atopic dermatitisEarly growth response 1Epidermal barrierHouse dust miteLipid metabolismRNA sequencing

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.