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生长抑素抑制人角质形成细胞的迁移并减少细胞数量,并在体外伤口模型中延迟表皮伤口愈合。

Somatostatin inhibits cell migration and reduces cell counts of human keratinocytes and delays epidermal wound healing in an ex vivo wound model.

机构信息

Department of Dermatology and Venerology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

出版信息

PLoS One. 2011 May 11;6(5):e19740. doi: 10.1371/journal.pone.0019740.

Abstract

The peptide hormone somatostatin (SST) and its five G protein-coupled receptors (SSTR1-5) were described to be present in the skin, but their cutaneous function(s) and skin-specific signalling mechanisms are widely unknown. By using receptor specific agonists we show here that the SSTRs expressed in keratinocytes are functionally coupled to the inhibition of adenylate cyclase. In addition, treatment with SSTR4 and SSTR5/1 specific agonists significantly influences the MAP kinase signalling pathway. As epidermal hormone receptors in general are known to regulate re-epithelialization following skin injury, we investigated the effect of SST on cell counts and migration of human keratinocytes. Our results demonstrate a significant inhibition of cell migration and reduction of cell counts by SST. We do not observe an effect on apoptosis and necrosis. Analysis of signalling pathways showed that somatostatin inhibits cell migration independent of its effect on cAMP. Migrating keratinocytes treated with SST show altered cytoskeleton dynamics with delayed lamellipodia formation. Furthermore, the activity of the small GTPase Rac1 is diminished, providing evidence for the control of the actin cytoskeleton by somatostatin receptors in keratinocytes. While activation of all receptors leads to redundant effects on cell migration, only treatment with a SSTR5/1 specific agonist resulted in decreased cell counts. In accordance with reduced cell counts and impaired migration we observe delayed re-epithelialization in an ex vivo wound healing model. Consequently, our experiments suggest SST as a negative regulator of epidermal wound healing.

摘要

多肽激素生长抑素 (SST) 及其五个 G 蛋白偶联受体 (SSTR1-5) 被描述存在于皮肤中,但它们在皮肤中的功能和皮肤特异性信号机制尚不清楚。通过使用受体特异性激动剂,我们在这里表明,角质形成细胞中表达的 SSTR 与腺苷酸环化酶的抑制功能偶联。此外,用 SSTR4 和 SSTR5/1 特异性激动剂处理可显著影响 MAP 激酶信号通路。由于一般来说表皮激素受体被认为可调节皮肤损伤后的再上皮化,我们研究了 SST 对人角质形成细胞计数和迁移的影响。我们的结果表明 SST 可显著抑制细胞迁移并减少细胞计数。我们没有观察到对细胞凋亡和坏死的影响。信号通路分析表明,SST 通过其对 cAMP 的作用抑制细胞迁移。用 SST 处理的迁移角质形成细胞显示出细胞骨架动力学改变,其片状伪足形成延迟。此外,小 GTPase Rac1 的活性降低,为 SST 受体在角质形成细胞中对肌动蛋白细胞骨架的控制提供了证据。虽然所有受体的激活都会导致细胞迁移的冗余效应,但只有用 SSTR5/1 特异性激动剂处理才会导致细胞计数减少。与细胞计数减少和迁移受损一致,我们在体外伤口愈合模型中观察到再上皮化延迟。因此,我们的实验表明 SST 是表皮伤口愈合的负调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a20f/3092774/b9fab0dd38cb/pone.0019740.g001.jpg

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