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D2-40在原发性瘢痕性和非瘢痕性脱发中的表达。

D2-40 expression in primary scarring and nonscarring alopecia.

作者信息

Mahalingam Meera, Hoang Mai P

机构信息

Dermatopathology Section, Department of Dermatology, Boston University School of Medicine, 609 Albany Street, Boston, MA 02118, USA.

出版信息

Am J Dermatopathol. 2010 Jul;32(5):427-31. doi: 10.1097/DAD.0b013e3181c34242.

DOI:10.1097/DAD.0b013e3181c34242
PMID:20414092
Abstract

The pathogenesis of scarring alopecia is believed to be related to damage to stem cells within, and outside the confines of, the follicular bulge region. Scattered reports indicate that D2-40, a monoclonal antibody that specifically detects a fixation-resistant epitope on podoplanin, highlights the basal cell layer of the outer root sheath. Given this, we sought to ascertain involvement of the same in a total of 52 cases of alopecia (33 scarring and 19 nonscarring). D2-40 expression, noted in the peripheral layer of the outer root sheath (above and below attachment of the pilar muscle), was similar in 24/33 (73%) and increased in 9/33 (27%) in the infundibular region of cases of scarring alopecia in comparison to its expression in 17/19 (90%; no expression noted in the other 2) of cases of nonscarring alopecia. The absence of a unifying diagnosis in entities demonstrating an increase precludes any correlation from being made regarding D2-40 expression and histologic diagnosis. However, more recently, podoplanin has been shown to be a novel Fos target gene in some skin cancers. Thus, from a scientific perspective, involvement of Fos-dependent transcription mechanisms in the etiopathogenesis of select scarring alopecias does not seem entirely unreasonable although studies defining the role of the Fos-podoplanin axis in development of the normal hair follicle are required before a definitive conclusion can be drawn.

摘要

瘢痕性脱发的发病机制被认为与毛囊隆突区内外的干细胞损伤有关。零散报道表明,D2-40(一种特异性检测血小板内皮细胞黏附分子上抗固定表位的单克隆抗体)可使外根鞘的基底细胞层显色。鉴于此,我们试图确定其在总共52例脱发患者(33例瘢痕性脱发和19例非瘢痕性脱发)中的作用。与19例非瘢痕性脱发患者中的17例(90%;另外2例未观察到表达)相比,瘢痕性脱发患者漏斗部区域外根鞘外周层(毛肌附着点上下)中观察到的D2-40表达,24/33(73%)相似,9/33(27%)增加。在显示表达增加的病例中缺乏统一诊断,这使得无法就D2-40表达与组织学诊断进行任何相关性分析。然而,最近已证明血小板内皮细胞黏附分子在某些皮肤癌中是一种新的Fos靶基因。因此,从科学角度来看,Fos依赖性转录机制参与某些瘢痕性脱发的发病机制似乎并非完全不合理,尽管在得出明确结论之前,需要开展研究来明确Fos-血小板内皮细胞黏附分子轴在正常毛囊发育中的作用。

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