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简明综述:人类多能干细胞生成肾脏。

Concise Review: Kidney Generation with Human Pluripotent Stem Cells.

机构信息

Department of Medicine, Renal Division, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Stem Cells. 2017 Nov;35(11):2209-2217. doi: 10.1002/stem.2699. Epub 2017 Sep 26.

Abstract

Chronic kidney disease (CKD) is a worldwide health care problem, resulting in increased cardiovascular mortality and often leading to end-stage kidney disease, where patients require kidney replacement therapies such as hemodialysis or kidney transplantation. Loss of functional nephrons contributes to the progression of CKD, which can be attenuated but not reversed due to inability to generate new nephrons in human adult kidneys. Human pluripotent stem cells (hPSCs), by virtue of their unlimited self-renewal and ability to differentiate into cells of all three embryonic germ layers, are attractive sources for kidney regenerative therapies. Recent advances in stem cell biology have identified key signals necessary to maintain stemness of human nephron progenitor cells (NPCs) in vitro, and led to establishment of protocols to generate NPCs and nephron epithelial cells from human fetal kidneys and hPSCs. Effective production of large amounts of human NPCs and kidney organoids will facilitate elucidation of developmental and pathobiological pathways, kidney disease modeling and drug screening as well as kidney regenerative therapies. We summarize the recent studies to induce NPCs and kidney cells from hPSCs, studies of NPC expansion from mouse and human embryonic kidneys, and discuss possible approaches in vivo to regenerate kidneys with cell therapies and the development of bioengineered kidneys. Stem Cells 2017;35:2209-2217.

摘要

慢性肾脏病(CKD)是一个全球性的医疗保健问题,导致心血管死亡率增加,并且常常导致终末期肾病,患者需要肾替代治疗,如血液透析或肾移植。功能性肾单位的丧失导致 CKD 的进展,由于人类成年肾脏无法产生新的肾单位,因此这种进展可以减轻但无法逆转。人类多能干细胞(hPSCs)由于其无限的自我更新能力和分化为三个胚胎胚层所有细胞的能力,是肾脏再生治疗的有吸引力的来源。干细胞生物学的最新进展确定了维持人类肾祖细胞(NPCs)体外干性所必需的关键信号,并导致建立了从人胎儿肾脏和 hPSCs 生成 NPCs 和肾上皮细胞的方案。大量有效产生的人 NPCs 和肾类器官将有助于阐明发育和病理生物学途径、肾脏疾病建模和药物筛选以及肾脏再生治疗。我们总结了最近从 hPSCs 诱导 NPCs 和肾细胞的研究、从小鼠和人胚胎肾脏中 NPC 扩增的研究,并讨论了体内用细胞疗法和生物工程肾脏再生肾脏的可能方法。干细胞 2017;35:2209-2217。

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