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Paligenosis: Cellular Remodeling During Tissue Repair
Annual Review of Physiology ( IF 18.2 ) Pub Date : 2022-02-10 , DOI: 10.1146/annurev-physiol-061121-035954
Jeffrey W Brown 1 , Charles J Cho 1, 2 , Jason C Mills 1, 2, 3, 4
Affiliation  

Complex multicellular organisms have evolved specific mechanisms to replenish cells in homeostasis and during repair. Here, we discuss how emerging technologies (e.g., single-cell RNA sequencing) challenge the concept that tissue renewal is fueled by unidirectional differentiation from a resident stem cell. We now understand that cell plasticity, i.e., cells adaptively changing differentiation state or identity, is a central tissue renewal mechanism. For example, mature cells can access an evolutionarily conserved program (paligenosis) to reenter the cell cycle and regenerate damaged tissue. Most tissues lack dedicated stem cells and rely on plasticity to regenerate lost cells. Plasticity benefits multicellular organisms, yet it also carries risks. For one, when long-lived cells undergo paligenotic, cyclical proliferation and redif-ferentiation, they can accumulate and propagate acquired mutations that activate oncogenes and increase the potential for developing cancer. Lastly, we propose a new framework for classifying patterns of cell proliferation in homeostasis and regeneration, with stem cells representing just one of the diverse methods that adult tissues employ.

中文翻译:


Paligenosis:组织修复过程中的细胞重塑

复杂的多细胞生物已经进化出特定的机制来补充体内平衡和修复过程中的细胞。在这里,我们讨论了新兴技术(例如,单细胞 RNA 测序)如何挑战组织更新是由常驻干细胞的单向分化推动的概念。我们现在了解到细胞可塑性,即细胞自适应地改变分化状态或身份,是一种主要的组织更新机制。例如,成熟细胞可以访问进化上保守的程序(paligenosis)以重新进入细胞周期并再生受损组织。大多数组织缺乏专门的干细胞,并依靠可塑性来再生丢失的细胞。可塑性有利于多细胞生物,但也存在风险。其一,当长寿细胞经历异源性、周期性增殖和再分化时,它们可以积累和传播获得性突变,激活致癌基因并增加患癌症的可能性。最后,我们提出了一个新的框架,用于对稳态和再生中的细胞增殖模式进行分类,干细胞只是成人组织采用的多种方法之一。

更新日期:2022-02-11
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