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皮肤中的p75神经营养因子受体:超越其神经营养功能

p75 Neurotrophin Receptor in the Skin: Beyond Its Neurotrophic Function.

作者信息

Pincelli Carlo

机构信息

Laboratory of Cutaneous Biology, Department of Surgical, Medical, Dental and Morphological Sciences, University of Modena and Reggio Emilia , Modena , Italy.

出版信息

Front Med (Lausanne). 2017 Mar 7;4:22. doi: 10.3389/fmed.2017.00022. eCollection 2017.

DOI:10.3389/fmed.2017.00022
PMID:28326307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5339601/
Abstract

p75 neurotrophin receptor (p75), 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 p75 is becoming more and more important. This review will focus on the intriguing functions of p75 in healthy and diseased skin. First, p75 counterbalances the proliferative and survival activities of its cognate receptor Trk by inducing keratinocyte apoptosis. In addition, p75 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. p75 is absent in psoriatic TA cells, thus rendering these cells resistant to apoptosis. On the other hand, p75 infection restores NT-induced apoptosis in psoriatic keratinocytes. Taken together, these results provide evidence for a critical role of p75 in epidermal homeostasis, while its lack may account for the TA defect in psoriasis. While the issue of p75 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 and . All in all, this review points to p75 as a major actor in both physiologic and pathologic conditions at the skin level.

摘要

p75神经营养因子受体(p75),也被称为CD271,是一种低亲和力受体,它与酪氨酸激酶受体原肌球蛋白受体激酶(Trk)共同介导神经营养因子(NT)的功能。除了在皮肤神经支配中的经典作用外,NT及其受体构成了一个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的作用变得越来越重要。本综述将聚焦于p75在健康和患病皮肤中的有趣功能。首先,p75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识别早期过渡扩增(TA)角质形成细胞群体,并在角质形成干细胞向其后代的转变以及表皮分化中起关键作用。p75在银屑病TA细胞中缺失,因此使这些细胞对凋亡具有抗性。另一方面,p75感染可恢复银屑病角质形成细胞中NT诱导的凋亡。综上所述,这些结果为p75在表皮稳态中的关键作用提供了证据,而其缺失可能是银屑病中TA缺陷的原因。虽然p75作为黑色素瘤起始细胞标志物的问题仍有待解决,但有强有力的证据表明该受体的下调是黑色素瘤侵袭和转移的先决条件。总而言之,本综述指出p75是皮肤水平生理和病理状况中的主要参与者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1915/5339601/71070dded7b4/fmed-04-00022-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1915/5339601/54c5792bce5e/fmed-04-00022-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1915/5339601/71070dded7b4/fmed-04-00022-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1915/5339601/54c5792bce5e/fmed-04-00022-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1915/5339601/71070dded7b4/fmed-04-00022-g002.jpg

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