Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Department of Kidney Regenerative Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Cell Rep. 2022 Jun 14;39(11):110933. doi: 10.1016/j.celrep.2022.110933.
Generation of new kidneys can be useful in various research fields, including organ transplantation. However, generating renal stroma, an important component tissue for structural support, endocrine function, and kidney development, remains difficult. Organ generation using an animal developmental niche can provide an appropriate in vivo environment for renal stroma differentiation. Here, we generate rat renal stroma with endocrine capacity by removing mouse stromal progenitor cells (SPCs) from the host developmental niche and transplanting rat SPCs. Furthermore, we develop a method to replace both nephron progenitor cells (NPCs) and SPCs, called the interspecies dual replacement of the progenitor (i-DROP) system, and successfully generate functional chimeric kidneys containing rat nephrons and stroma. This method can generate renal tissue from progenitors and reduce xenotransplant rejection. Moreover, it is a safe method, as donor cells do not stray into nontarget organs, thus accelerating research on stem cells, chimeras, and xenotransplantation.
生成新的肾脏在各个研究领域都很有用,包括器官移植。然而,生成肾基质,一种用于结构支持、内分泌功能和肾脏发育的重要组织成分,仍然很困难。利用动物发育小生境生成器官可以为肾基质分化提供合适的体内环境。在这里,我们通过从宿主发育小生境中去除小鼠基质祖细胞(SPC)并移植大鼠 SPC 来生成具有内分泌能力的大鼠肾基质。此外,我们开发了一种方法来替代肾祖细胞(NPC)和 SPC,称为种间祖细胞双重替代(i-DROP)系统,并成功生成了含有大鼠肾单位和基质的功能性嵌合肾脏。该方法可以从祖细胞生成肾脏组织并减少异种移植排斥反应。此外,这是一种安全的方法,因为供体细胞不会误入非靶器官,从而加速干细胞、嵌合体和异种移植的研究。