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Improved Sendai viral system for reprogramming to naive pluripotency.改良的仙台病毒系统用于重编程为原始多能性。
Cell Rep Methods. 2022 Oct 17;2(11):100317. doi: 10.1016/j.crmeth.2022.100317. eCollection 2022 Nov 21.
2
Spotlighting adult stem cells: advances, pitfalls, and challenges.聚焦成人干细胞:进展、陷阱和挑战。
Trends Cell Biol. 2023 Jun;33(6):477-494. doi: 10.1016/j.tcb.2022.09.007. Epub 2022 Oct 18.
3
Induction of a NOTCH3 Lehman syndrome mutation in osteocytes causes osteopenia in male C57BL/6J mice.诱导成骨细胞中 NOTCH3 Lehman 综合征突变导致雄性 C57BL/6J 小鼠出现骨质疏松症。
Bone. 2022 Sep;162:116476. doi: 10.1016/j.bone.2022.116476. Epub 2022 Jun 26.
4
Cas9-induced large deletions and small indels are controlled in a convergent fashion.Cas9 诱导的大片段缺失和小片段插入以收敛的方式被控制。
Nat Commun. 2022 Jun 14;13(1):3422. doi: 10.1038/s41467-022-30480-8.
5
Mending the gaps: ethically sensitive cells and the evolution of European stem cell policy.弥合差距:伦理敏感细胞与欧洲干细胞政策的演变。
Regen Med. 2022 Aug;17(8):581-595. doi: 10.2217/rme-2022-0043. Epub 2022 Jun 7.
6
Skeletal disorders associated with the growth hormone-insulin-like growth factor 1 axis.与生长激素-胰岛素样生长因子 1 轴相关的骨骼疾病。
Nat Rev Endocrinol. 2022 Jun;18(6):353-365. doi: 10.1038/s41574-022-00649-8. Epub 2022 Mar 14.
7
Early human embryonic development: Blastocyst formation to gastrulation.早期人类胚胎发育:囊胚形成至原肠胚形成。
Dev Cell. 2022 Jan 24;57(2):152-165. doi: 10.1016/j.devcel.2021.12.022.
8
Quantitative Craniofacial Analysis and Generation of Human Induced Pluripotent Stem Cells for Muenke Syndrome: A Case Report.孟克综合征的定量颅面分析及人诱导多能干细胞的生成:病例报告
J Dev Biol. 2021 Sep 22;9(4):39. doi: 10.3390/jdb9040039.
9
Deletion and replacement of long genomic sequences using prime editing.使用 Prime Editing 进行长基因组序列的删除和替换。
Nat Biotechnol. 2022 Feb;40(2):227-234. doi: 10.1038/s41587-021-01026-y. Epub 2021 Oct 14.
10
Human iPS-derived pre-epicardial cells direct cardiomyocyte aggregation expansion and organization in vitro.人诱导多能干细胞衍生的原始心外膜细胞在体外指导心肌细胞的聚集、扩增和组织。
Nat Commun. 2021 Aug 17;12(1):4997. doi: 10.1038/s41467-021-24921-z.

诱导多能干细胞技术在骨生物学中的应用。

Induced pluripotent stem cell technology in bone biology.

机构信息

Skeletal Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892, United States of America.

Center for Skeletal Research, Orthopedic Surgery and Medicine, UConn Musculoskeletal Institute, UConn Health, Farmington, CT 06030-4037, United States of America.

出版信息

Bone. 2023 Jul;172:116760. doi: 10.1016/j.bone.2023.116760. Epub 2023 Apr 6.

DOI:10.1016/j.bone.2023.116760
PMID:37028583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10228209/
Abstract

Technologies on the development and differentiation of human induced pluripotent stem cells (hiPSCs) are rapidly improving, and have been applied to create cell types relevant to the bone field. Differentiation protocols to form bona fide bone-forming cells from iPSCs are available, and can be used to probe details of differentiation and function in depth. When applied to iPSCs bearing disease-causing mutations, the pathogenetic mechanisms of diseases of the skeleton can be elucidated, along with the development of novel therapeutics. These cells can also be used for development of cell therapies for cell and tissue replacement.

摘要

人类诱导多能干细胞(hiPSCs)的开发和分化技术正在迅速发展,并已应用于创建与骨骼领域相关的细胞类型。现在已有从 iPSCs 形成真正的成骨细胞的分化方案,并可用于深入探究分化和功能的细节。当应用于携带致病突变的 iPSCs 时,可以阐明骨骼疾病的发病机制,并开发新的治疗方法。这些细胞还可用于开发用于细胞和组织替代的细胞疗法。