A gene edited pig model for studying LGR5+ stem cells: implications for future applications in tissue regeneration and biomedical research

IF 4.9 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Frontiers in genome editing Pub Date : 2024-06-06 DOI:10.3389/fgeed.2024.1401163
Amanda B. T. Hill, Yanet Murphy, K. Polkoff, Laura Edwards, Derek M. Walker, A. Moatti, A. Greenbaum, Jorge A. Piedrahita
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Abstract

Recent advancements in genome editing techniques, notably CRISPR-Cas9 and TALENs, have marked a transformative era in biomedical research, significantly enhancing our understanding of disease mechanisms and helping develop novel therapies. These technologies have been instrumental in creating precise animal models for use in stem cell research and regenerative medicine. For instance, we have developed a transgenic pig model to enable the investigation of LGR5-expressing cells. The model was designed to induce the expression of H2B-GFP under the regulatory control of the LGR5 promoter via CRISPR/Cas9-mediated gene knock-in. Notably, advancements in stem cell research have identified distinct subpopulations of LGR5-expressing cells within adult human, mouse, and pig tissues. LGR5, a leucine-rich repeat-containing G protein-coupled receptor, enhances WNT signaling and these LGR5+ subpopulations demonstrate varied roles and anatomical distributions, underscoring the necessity for suitable translational models. This transgenic pig model facilitates the tracking of LGR5-expressing cells and has provided valuable insights into the roles of these cells across different tissues and species. For instance, in pulmonary tissue, Lgr5+ cells in mice are predominantly located in alveolar compartments, driving alveolar differentiation of epithelial progenitors via Wnt pathway activation. In contrast, in pigs and humans, these cells are situated in a unique sub-basal position adjacent to the airway epithelium. In fetal stages a pattern of LGR5 expression during lung bud tip formation is evident in humans and pigs but is lacking in mice. Species differences with respect to LGR5 expression have also been observed in the skin, intestines, and cochlea further reinforcing the need for careful selection of appropriate translational animal models. This paper discusses the potential utility of the LGR5+ pig model in exploring the role of LGR5+ cells in tissue development and regeneration with the goal of translating these findings into human and animal clinical applications.
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研究 LGR5+ 干细胞的基因编辑猪模型:对未来组织再生和生物医学研究应用的影响
基因组编辑技术(特别是 CRISPR-Cas9 和 TALENs)的最新进展标志着生物医学研究进入了一个变革时代,极大地增强了我们对疾病机制的了解,并有助于开发新型疗法。这些技术在创建用于干细胞研究和再生医学的精确动物模型方面发挥了重要作用。例如,我们开发了一种转基因猪模型,用于研究LGR5表达细胞。该模型旨在通过CRISPR/Cas9介导的基因敲入,在LGR5启动子的调控下诱导H2B-GFP的表达。值得注意的是,干细胞研究的进步已经在成人人类、小鼠和猪组织中发现了不同的LGR5表达细胞亚群。LGR5是一种富含亮氨酸重复的G蛋白偶联受体,能增强WNT信号转导,这些LGR5+亚群表现出不同的作用和解剖学分布,强调了建立合适的转化模型的必要性。这种转基因猪模型有助于跟踪 LGR5 表达细胞,并为了解这些细胞在不同组织和物种中的作用提供了宝贵的见解。例如,在肺组织中,小鼠的 Lgr5+ 细胞主要位于肺泡区,通过 Wnt 通路的激活驱动上皮祖细胞的肺泡分化。相反,在猪和人体内,这些细胞位于独特的基底下位置,与气道上皮相邻。在人和猪的胎儿阶段,肺芽尖端形成过程中的 LGR5 表达模式非常明显,但小鼠却缺乏这种表达模式。在皮肤、肠道和耳蜗中也观察到了 LGR5 表达的物种差异,这进一步加强了仔细选择合适的转化动物模型的必要性。本文讨论了 LGR5+ 猪模型在探索 LGR5+ 细胞在组织发育和再生中的作用方面的潜在用途,目的是将这些发现转化为人类和动物的临床应用。
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7.00
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0.00%
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审稿时长
13 weeks
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