默克尔细胞分化的分子调控机制。

IF 11.7 1区 生物学 Q1 BIOLOGY
Christian Felice Cervellera, Chiara Mazziotta, Elisa Mazzoni, Ilaria Bononi, Maria Rosa Iaquinta, Mauro Tognon, Fernanda Martini, John Charles Rotondo
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引用次数: 0

摘要

默克尔细胞是一种特殊的卵形上皮细胞,位于基底表皮和毛囊中,与负责轻触感觉的传入神经末梢相连。发育生物学的最新进展揭示了控制默克尔细胞成熟的复杂调控网络。最近的证据表明,表观遗传途径之间存在串扰,特别是Polycomb多亚基复合物,默克尔细胞系转录因子,如无调性BHLH转录因子1 (ATOH1), SRY-box转录因子2 (SOX2), ISL LIM同源盒1 (ISL1)和调节默克尔细胞发育程序的其他参与者。同时,默克尔细胞癌(MCC)发病过程中默克尔细胞谱系转录因子失调的影响正在研究中。本文综述了目前对默克尔细胞分化至关重要的遗传和表观遗传途径的理解。它涵盖了默克尔细胞特异性发育程序的含义,表观遗传调控多梳复合物的作用,以及遗传和表观遗传机制如何汇聚以协调默克尔细胞分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular regulatory mechanisms of Merkel cell differentiation.

Merkel cells are specialized oval-shaped epithelial cells located in the basal epidermis and hair follicles, connected with afferent nerve endings responsible for sensory perception of light touch. Recent advances in developmental biology have shed light on the complex regulatory networks governing Merkel cell maturation. The most recent evidence indicates a crosstalk among epigenetic pathways, notably Polycomb multi-subunit complexes, Merkel cell-lineage transcription factors such as atonal BHLH transcription factor 1 (ATOH1), SRY-box transcription factor 2 (SOX2), ISL LIM homeobox 1 (ISL1) and additional players in the regulation of Merkel cell developmental programs. At the same time, the implications of dysregulated Merkel cell-lineage transcription factors during Merkel cell carcinoma (MCC) onset is under investigation. This review offers a comprehensive overview of the current understanding of the genetic and epigenetic pathways crucial for Merkel cell differentiation. It covers the implication of Merkel cell-specific developmental programs, the role of epigenetic regulatory Polycomb complexes, and how genetic and epigenetic mechanisms converge to orchestrate Merkel cell differentiation.

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来源期刊
Biological Reviews
Biological Reviews 生物-生物学
CiteScore
21.30
自引率
2.00%
发文量
99
审稿时长
6-12 weeks
期刊介绍: Biological Reviews is a scientific journal that covers a wide range of topics in the biological sciences. It publishes several review articles per issue, which are aimed at both non-specialist biologists and researchers in the field. The articles are scholarly and include extensive bibliographies. Authors are instructed to be aware of the diverse readership and write their articles accordingly. The reviews in Biological Reviews serve as comprehensive introductions to specific fields, presenting the current state of the art and highlighting gaps in knowledge. Each article can be up to 20,000 words long and includes an abstract, a thorough introduction, and a statement of conclusions. The journal focuses on publishing synthetic reviews, which are based on existing literature and address important biological questions. These reviews are interesting to a broad readership and are timely, often related to fast-moving fields or new discoveries. A key aspect of a synthetic review is that it goes beyond simply compiling information and instead analyzes the collected data to create a new theoretical or conceptual framework that can significantly impact the field. Biological Reviews is abstracted and indexed in various databases, including Abstracts on Hygiene & Communicable Diseases, Academic Search, AgBiotech News & Information, AgBiotechNet, AGRICOLA Database, GeoRef, Global Health, SCOPUS, Weed Abstracts, and Reaction Citation Index, among others.
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