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Expression and regulation of GPAT isoforms in cultured human keratinocytes and rodent epidermis

机译:GPAT亚型在培养的人角质形成细胞和啮齿动物表皮中的表达和调控

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摘要

Phospholipids are required for epidermal lamellar body formation. Glycerol 3-phosphate acyltransferases (GPATs) catalyze the initial step in the biosynthesis of glycerolipids. Little is known about the expression and regulation of GPATs in epidermis/keratinocytes. Here, we demonstrate that GPAT 1, 3, and 4 are expressed in epidermis/keratinocytes, whereas GPAT2 is not detected. In mouse epidermis, GPAT 3 and 4 are mainly localized to the upper layers whereas GPAT1 is found in both the upper and lower layers. GPAT1 and 3 mRNA increase during fetal rat epidermal development. No change in GPAT expression was observed in adult mice following acute permeability barrier disruption. Calcium-induced human keratinocyte differentiation increased GPAT3 mRNA whereas both GPAT1 and 4 mRNA levels decreased. In parallel, total GPAT activity increased 2-fold in differentiated keratinocytes attributable to an increase in N-ethylmaleimide (NEM) sensitive GPAT activity localized to microsomes with little change in NEM resistant activity, consistent with an increase in GPAT3. Furthermore, PPARγ or PPARδ activators increased GPAT3 mRNA, microsomal GPAT activity, and glycerol lipid synthesis without affecting the expression of GPAT1 or 4. Finally, both PPARγ and PPARδ activators increased GPAT3 mRNA via increasing its transcription. Thus, multiple isoforms of GPAT are expressed and differentially regulated in epidermis/keratinocytes.
机译:磷脂是表皮层状体形成所必需的。 3-磷酸​​甘油酰基转移酶(GPAT)催化甘油脂生物合成中的第一步。关于表皮/角质形成细胞中GPAT的表达和调控知之甚少。在这里,我们证明了GPAT 1、3和4在表皮/角质形成细胞中表达,而未检测到GPAT2。在小鼠表皮中,GPAT 3和4主要位于上层,而GPAT1在上层和下层中都发现。胎鼠表皮发育过程中,GPAT1和3 mRNA升高。急性通透性屏障破坏后,在成年小鼠中未观察到GPAT表达的变化。钙诱导的人类角质形成细胞分化增加GPAT3 mRNA,而GPAT1和4 mRNA水平均下降。同时,总的GPAT活性在分化的角质形成细胞中增加了2倍,这归因于N-乙基马来酰亚胺(NEM)敏感的GPAT活性的增加,该活性定位于微粒体,NEM抗性活性几乎没有变化,与GPAT3的增加一致。此外,PPARγ或PPARδ激活剂可增加GPAT3 mRNA,微粒体GPAT活性和甘油脂质合成,而不会影响GPAT1或4的表达。最后,PPARγ和PPARδ激活剂均通过增加其转录来增加GPAT3 mRNA。因此,GPAT的多种同工型在表皮/角质形成细胞中表达并受到不同的调节。

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