Purinergic Signaling and its Role in the Stem Cell Differentiation.

IF 3.3 3区 医学 Q2 CHEMISTRY, MEDICINAL Mini reviews in medicinal chemistry Pub Date : 2024-01-01 DOI:10.2174/0113895575261206231003151416
Sumera Zaib, Areeba, Imtiaz Khan
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Abstract

Purinergic signaling is a mechanism in which extracellular purines and pyrimidines interact with specialized cell surface receptors known as purinergic receptors. These receptors are divided into two families of P1 and P2 receptors, each responding to different nucleosides and nucleotides. P1 receptors are activated by adenosine, while P2 receptors are activated by pyrimidine and purines. P2X receptors are ligand-gated ion channels, including seven subunits (P2X1-7). However, P2Y receptors are the G-protein coupled receptors comprising eight subtypes (P2Y1/2/4/6/11/12/13/14). The disorder in purinergic signaling leads to various health-related issues and diseases. In various aspects, it influences the activity of non-neuronal cells and neurons. The molecular mechanism of purinergic signaling provides insight into treating various human diseases. On the contrary, stem cells have been investigated for therapeutic applications. Purinergic signaling has shown promising effect in stem cell engraftment. The immune system promotes the autocrine and paracrine mechanisms and releases the significant factors essential for successful stem cell therapy. Each subtype of purinergic receptor exerts a beneficial effect on the damaged tissue. The most common effect caused by purinergic signaling is the proliferation and differentiation that treat different health-related conditions.

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嘌呤能信号传导及其在干细胞分化中的作用。
嘌呤能信号传导是细胞外嘌呤和嘧啶与被称为嘌呤能受体的特殊细胞表面受体相互作用的一种机制。这些受体分为P1和P2受体的两个家族,每个家族对不同的核苷和核苷酸有反应。P1受体被腺苷激活,而P2受体被嘧啶和嘌呤激活。P2X受体是配体门控的离子通道,包括七个亚基(P2X1-7)。然而,P2Y受体是包含八种亚型(P2Y1/2/4/6/11/12/13/14)的G蛋白偶联受体。嘌呤能信号的紊乱会导致各种与健康相关的问题和疾病。在各个方面,它影响非神经元细胞和神经元的活动。嘌呤能信号传导的分子机制为治疗各种人类疾病提供了见解。相反,干细胞已被研究用于治疗应用。嘌呤能信号在干细胞移植中显示出良好的效果。免疫系统促进自分泌和旁分泌机制,并释放干细胞治疗成功所必需的重要因素。嘌呤能受体的每种亚型都对受损组织产生有益作用。嘌呤能信号传导引起的最常见影响是治疗不同健康状况的增殖和分化。
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来源期刊
CiteScore
7.80
自引率
0.00%
发文量
231
审稿时长
6 months
期刊介绍: The aim of Mini-Reviews in Medicinal Chemistry is to publish short reviews on the important recent developments in medicinal chemistry and allied disciplines. Mini-Reviews in Medicinal Chemistry covers all areas of medicinal chemistry including developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, drug targets, and natural product research and structure-activity relationship studies. Mini-Reviews in Medicinal Chemistry is an essential journal for every medicinal and pharmaceutical chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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