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克隆形成细胞亚群维持先天性黑素细胞痣。

Clonogenic cell subpopulations maintain congenital melanocytic nevi.

机构信息

Saint Antoine Research Center, U938, Institut National de la Santé et de la Recherche Médicale (INSERM), Paris, France; Université Pierre et Marie Curie-Paris VI, Paris, France.

Université René Descartes-Paris V, Paris, France; Department of Maxillofacial and Plastic Surgery, Hôpital Necker, Publique-Hôpitaux de Paris, Paris, France.

出版信息

J Invest Dermatol. 2015 Mar;135(3):824-833. doi: 10.1038/jid.2014.437. Epub 2014 Oct 13.

Abstract

Large congenital melanocytic nevi (lCMN) are benign melanocytic tumors associated with an increased risk of melanoma transformation. They result predominantly from a post-zygotic somatic NRAS mutation. These lesions persist and even increase after birth proportionally to the child's growth. Therefore, we asked here whether cells with clonogenic and tumorigenic properties persisted postnatally in lCMN. Subpopulations of lCMN cells expressed stem cell/progenitor lineage markers such as Sox10, Nestin, Oct4, and ABCB5. In vitro, 1 in 250 cells from fresh lCMN formed colonies that could be passaged and harbored the same NRAS mutation as the original nevus. In vivo, lCMN specimens xenografted in immunocompromised mice expanded 4-fold. BrdU(+)-proliferating and label-retaining melanocytes were found within the outgrowth skin tissue of these xenografts, which displayed the same benign nested architecture as the original nevus. lCMN cell suspensions were not able to expand when xenografted alone in Rag 2-/- mice. Conversely, when mixed with keratinocytes, these cells reconstituted the architecture of the human nevus with its characteristic melanocyte layout, lentiginous hyperplasia, and nested architecture. Overall, our data demonstrate that, after birth, certain lCMN cell subtypes still display features such as clonogenic potential and expand into nevus-like structures when cooperating with adjacent keratinocytes.

摘要

先天性巨痣(lCMN)是一种良性黑素细胞肿瘤,与黑色素瘤转化的风险增加有关。它们主要是由合子后体细胞 NRAS 突变引起的。这些病变在出生后会持续存在,甚至会随着孩子的生长而按比例增加。因此,我们在这里询问了在 lCMN 中是否存在具有克隆形成和致瘤性的细胞在出生后持续存在。lCMN 细胞的亚群表达干细胞/祖细胞谱系标志物,如 Sox10、Nestin、Oct4 和 ABCB5。在体外,新鲜 lCMN 中有 1/250 的细胞形成可以传代的集落,并携带与原始痣相同的 NRAS 突变。在体内,lCMN 标本异种移植到免疫缺陷小鼠中会扩大 4 倍。在这些异种移植物的生长皮肤组织中发现了 BrdU(+)增殖和标记保留的黑素细胞,其显示出与原始痣相同的良性巢状结构。当单独异种移植到 Rag2-/- 小鼠中时,lCMN 细胞悬浮液不能扩增。相反,当与角质形成细胞混合时,这些细胞会重建具有特征性黑素细胞排列、痣样增生和巢状结构的人类痣的结构。总体而言,我们的数据表明,出生后,某些 lCMN 细胞亚型仍表现出克隆形成潜力等特征,并与相邻角质形成细胞合作时会扩展为痣样结构。

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