Interdisciplinary Excellence Centre, Department of Microbiology, University of Szeged, Szeged, Hungary.
MTA-SZTE "Lendület" "Mycobiome" Research Group, University of Szeged, Szeged, Hungary.
Virulence. 2019 Dec;10(1):970-975. doi: 10.1080/21505594.2018.1559674. Epub 2019 Jan 7.
Eicosanoids are bioactive lipid mediators generated in almost all mammalian cells from the oxidation of arachidonic acid and other related twenty-carbon polyunsaturated fatty acids (PUFA). Eicosanoids regulate various physiological functions, including cellular homoeostasis and modulation of inflammatory responses in mammals. The mode of action of these lipid mediators depend on their binding to different G-protein coupled receptors. The three main enzymatic pathways associated with their production are the COX pathway, LOX pathway and cytochrome P450 pathway. Interestingly, investigations have also revealed that several human pathogenic fungi are capable of producing these bioactive lipid mediators; however, the exact biosynthetic pathways and their function in pathogenicity are not yet extensively characterized. The aim of the current review is to summarize the recent discoveries pertaining to eicosanoid production by human pathogenic yeasts with a special focus on the opportunistic human fungal pathogen .
类二十烷酸是生物活性脂质介质,几乎存在于所有哺乳动物细胞中,由花生四烯酸和其他相关的二十碳多不饱和脂肪酸(PUFA)氧化生成。类二十烷酸调节各种生理功能,包括哺乳动物细胞内稳态和炎症反应的调节。这些脂质介质的作用模式取决于它们与不同 G 蛋白偶联受体的结合。与它们的产生相关的三种主要酶促途径是 COX 途径、LOX 途径和细胞色素 P450 途径。有趣的是,研究还表明,几种人类致病真菌能够产生这些生物活性脂质介质;然而,其确切的生物合成途径及其在致病性中的作用尚未得到广泛描述。本综述的目的是总结与人类致病酵母产生类二十烷酸有关的最新发现,特别关注机会性人类真菌病原体。