Division of Gastroenterology, Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, Missouri, USA.
Current affiliation: Section of Gastroenterology and Hepatology, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA.
Annu Rev Physiol. 2022 Feb 10;84:461-483. doi: 10.1146/annurev-physiol-061121-035954. Epub 2021 Oct 27.
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.
复杂的多细胞生物已经进化出特定的机制来在体内平衡和修复过程中补充细胞。在这里,我们讨论新兴技术(例如单细胞 RNA 测序)如何挑战组织更新是由驻留干细胞单向分化驱动的概念。我们现在知道,细胞可塑性,即细胞适应性地改变分化状态或身份,是中央组织更新机制。例如,成熟细胞可以利用进化上保守的程序(返老还童)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,依赖可塑性来再生丢失的细胞。可塑性有益于多细胞生物,但也存在风险。一方面,当长寿细胞经历返老还童、周期性增殖和再分化时,它们可以积累和传播获得性突变,激活癌基因并增加发展癌症的潜力。最后,我们提出了一个新的框架来分类体内平衡和再生中细胞增殖的模式,其中干细胞仅代表成年组织采用的多种方法之一。