The emerging role of PKM in keratinocyte homeostasis and pathophysiology

被引:5
作者
Demeter, Jenna B. B. [1 ]
Elshaarrawi, Ahmed [2 ]
Dowker-Key, Presley D. D. [1 ]
Bettaieb, Ahmed [1 ,2 ,3 ,4 ]
机构
[1] Univ Tennessee, Dept Nutr, Knoxville, TN USA
[2] Univ Tennessee, Grad Sch Genome Sci & Technol, Knoxville, TN USA
[3] Univ Tennessee, Dept Biochem & Cellular & Mol Biol, Knoxville, TN USA
[4] Univ Tennessee, Dept Nutr, 1215 Cumberland Ave,229 Jessie Harris Bldg, Knoxville, TN 37996 USA
关键词
CRISPR/Cas9; system; gene editing; glycolysis; inflammation; keratinocytes; PKM1; PKM2; proliferation; psoriasis; ACTIVATED PROTEIN-KINASE; PYRUVATE-KINASE; CONTACT-DERMATITIS; AEROBIC GLYCOLYSIS; CANCER METABOLISM; SHIKONIN; M2; GLUTAMINE; ISOFORM; PROMOTE;
D O I
10.1111/febs.16700
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Increased aerobic glycolysis in keratinocytes has been reported as a hallmark of skin diseases while its pharmacological inhibition restores keratinocyte homeostasis. Pyruvate kinase muscle (PKM) isoforms are key enzymes in the glycolytic pathway and, therefore, an attractive therapeutic target. Simon Nold and colleagues used CRISPR/Cas9-mediated gene editing to investigate the outcomes of PKM splicing perturbations and specific PKM1 or PKM2 deficiency in human HaCaT keratinocytes. Collectively, the study demonstrated different effects of PKM1 or PKM2 depletion on the reciprocal PKM isoform and on keratinocyte gene expression, metabolism and proliferation. Findings from this study provide novel insights into the role of PKM in keratinocyte homeostasis, warranting additional investigations into the underlying molecular mechanisms and potential therapeutic applications.
引用
收藏
页码:2311 / 2319
页数:9
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