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p75 Neurotrophin Receptor in the Skin: Beyond Its Neurotrophic Function

机译:皮肤中的p75神经营养蛋白受体:超越其神经营养功能

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摘要

p75 neurotrophin receptor (p75NTR), also known as CD271, is the low-affinity receptor that, together with the tyrosine kinase receptor tropomyosin-receptor kinase (Trk), mediate neurotrophin (NT) functions. Beside their classic role in skin innervation, NT and their receptors constitute a complex cutaneous network associated with a number of autocrine and paracrine activities. In this context, the role of p75NTR is becoming more and more important. This review will focus on the intriguing functions of p75NTR in healthy and diseased skin. First, p75NTR counterbalances the proliferative and survival activities of its cognate receptor Trk by inducing keratinocyte apoptosis. In addition, p75NTR identifies an early transit-amplifying (TA) keratinocyte population and plays a critical role in keratinocyte stem cell transition to its progeny as well as in epidermal differentiation. p75NTR is absent in psoriatic TA cells, thus rendering these cells resistant to apoptosis. On the other hand, p75NTR infection restores NT-induced apoptosis in psoriatic keratinocytes. Taken together, these results provide evidence for a critical role of p75NTR in epidermal homeostasis, while its lack may account for the TA defect in psoriasis. While the issue of p75NTR as a marker of melanoma initiating cells is still to be solved, there is strong evidence that downregulation of this receptor is a precondition to melanoma invasion and metastasis in vitro and in vivo. All in all, this review points to p75NTR as a major actor in both physiologic and pathologic conditions at the skin level.
机译:p75神经营养蛋白受体(p75 NTR ),也称为CD271,是一种低亲和力受体,与酪氨酸激酶受体原肌球蛋白受体激酶(Trk)一起介导神经营养蛋白(NT)的功能。除了其在皮肤神经支配中的经典作用外,NT及其受体还构成了与许多自分泌和旁分泌活动相关的复杂皮肤网络。在这种情况下,p75 NTR 的作用变得越来越重要。本文将重点探讨p75 NTR 在健康和患病皮肤中的有趣功能。首先,p75 NTR 通过诱导角质形成细胞凋亡来平衡其同源受体Trk的增殖和存活活性。此外,p75 NTR 可以识别早期转运扩增(TA)角质形成细胞,并在角质形成干细胞向其后代过渡以及表皮分化中发挥关键作用。银屑病TA细胞中不存在p75 NTR ,因此使这些细胞对细胞凋亡具有抗性。另一方面,p75 NTR 感染可恢复NT诱导的银屑病角质形成细胞凋亡。综上所述,这些结果提供了p75 NTR 在表皮稳态中的关键作用的证据,而其缺乏可能解释了牛皮癣的TA缺陷。尽管p75 NTR 作为黑色素瘤起始细胞的标志物的问题仍待解决,但有力的证据表明,该受体的下调是体内外黑色素瘤侵袭和转移的前提。总而言之,这篇评论指出p75 NTR 是皮肤水平上生理和病理状况的主要参与者。

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