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设计人类组织:即将走进你身边的实验室。

Designer human tissue: coming to a lab near you.

机构信息

MRC Centre for Regenerative Medicine, University of Edinburgh, 5 Little France Drive, EH16 4UU Edinburgh, UK

Trinity Biomedical Sciences Institute, Trinity College Dublin, 152-160 Pearse St, Dublin 2, Dublin, Republic of Ireland.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0212.

DOI:10.1098/rstb.2017.0212
PMID:29786548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5974436/
Abstract

Human pluripotent stem cells (PSCs) offer a scalable alternative to primary and transformed human tissue. PSCs include human embryonic stem cells, derived from the inner cell mass of blastocysts unsuitable for human implantation; and induced PSCs, generated by the reprogramming of somatic cells. Both cell types display the ability to self-renew and retain pluripotency, promising an unlimited supply of human somatic cells for biomedical application. A distinct advantage of using PSCs is the ability to select for genetic background, promising personalized modelling of human biology 'in a dish' or immune-matched cell-based therapies for the clinic. This special issue will guide the reader through stem cell self-renewal, pluripotency and differentiation. The first articles focus on improving cell fidelity, understanding the innate immune system and the importance of materials chemistry, biofabrication and bioengineering. These are followed by articles that focus on industrial application, commercialization and label-free assessment of tissue formation. The special issue concludes with an article discussing human liver cell-based therapies past, present and future.This article is part of the theme issue 'Designer human tissue: coming to a lab near you'.

摘要

人类多能干细胞(PSCs)为原发性和转化性人体组织提供了一种可扩展的替代方法。PSCs 包括人类胚胎干细胞,来源于不适宜人类植入的囊胚内细胞团;以及通过体细胞重编程产生的诱导多能干细胞。这两种细胞类型都具有自我更新和保持多能性的能力,有望为生物医学应用提供无限供应的人类体细胞。使用 PSCs 的一个明显优势是能够选择遗传背景,有望在“体外”对人类生物学进行个性化建模,或为临床提供免疫匹配的基于细胞的治疗方法。本期特刊将引导读者了解干细胞自我更新、多能性和分化。前几篇文章重点介绍了提高细胞保真度、了解固有免疫系统以及材料化学、生物制造和生物工程的重要性。随后的文章则侧重于工业应用、商业化和无标记组织形成评估。本期特刊以一篇讨论过去、现在和未来基于人类肝细胞的治疗方法的文章结束。

这篇文章是主题特刊“设计人类组织:即将在您附近的实验室出现”的一部分。

相似文献

1
Designer human tissue: coming to a lab near you.设计人类组织:即将走进你身边的实验室。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0212.
2
Pluripotent stem cells: induction and self-renewal.多能干细胞:诱导与自我更新。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0213.
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From skeletal development to the creation of pluripotent stem cell-derived bone-forming progenitors.从骨骼发育到多能干细胞衍生的成骨祖细胞的创建。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0218.
4
The use of pluripotent stem cell for personalized cell therapies against neurological disorders.使用多能干细胞进行针对神经疾病的个性化细胞治疗。
J Biomed Biotechnol. 2011;2011:520816. doi: 10.1155/2011/520816. Epub 2011 Dec 13.
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Human parthenogenetic embryonic stem cells: one potential resource for cell therapy.人类孤雌生殖胚胎干细胞:细胞治疗的一种潜在资源。
Sci China C Life Sci. 2009 Jul;52(7):599-602. doi: 10.1007/s11427-009-0096-2. Epub 2009 Jul 30.
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Generation of defined neural populations from pluripotent stem cells.从多能干细胞中生成定义明确的神经群体。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0214.
7
The cell cycle and pluripotency.细胞周期与多能性。
Biochem J. 2013 Apr 15;451(2):135-43. doi: 10.1042/BJ20121627.
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Three-dimensional cell culture: from evolution to revolution.三维细胞培养:从进化到革命。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0216.
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Advances in culture and manipulation of human pluripotent stem cells.人类多能干细胞的培养和操作技术的新进展
J Dent Res. 2013 Nov;92(11):956-62. doi: 10.1177/0022034513501286. Epub 2013 Aug 9.
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Efficient induction and sustenance of pluripotent stem cells from bovine somatic cells.高效诱导牛体细胞多能干细胞并维持其多能性。
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本文引用的文献

1
Modelling non-alcoholic fatty liver disease in human hepatocyte-like cells.在人源肝样细胞中建立非酒精性脂肪性肝病模型。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0362.
2
Developing defined substrates for stem cell culture and differentiation.开发用于干细胞培养和分化的定义明确的基质。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0230.
3
Cell-based liver therapies: past, present and future.基于细胞的肝脏治疗:过去、现在和未来。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0229.
4
Application of hepatocyte-like cells to enhance hepatic safety risk assessment in drug discovery.肝细胞样细胞在药物发现中增强肝安全性风险评估的应用。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0228.
5
Impedance-based cellular assays for regenerative medicine.基于阻抗的再生医学细胞检测法。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0226.
6
Microfabrication of liver and heart tissues for drug development.用于药物开发的肝和心脏组织的微加工。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0225.
7
Three-dimensional bioprinting of stem-cell derived tissues for human regenerative medicine.基于干细胞的组织的三维生物打印用于人类再生医学。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0224.
8
New substrates for stem cell control.干细胞控制的新基质。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0223.
9
The gene regulatory network of mESC differentiation: a benchmark for reverse engineering methods.胚胎干细胞分化的基因调控网络:反向工程方法的基准。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0222.
10
Assessment of stem cell differentiation based on genome-wide expression profiles.基于全基因组表达谱的干细胞分化评估。
Philos Trans R Soc Lond B Biol Sci. 2018 Jul 5;373(1750). doi: 10.1098/rstb.2017.0221.