Phenotypic technologies in stem cell biology.

Phenotypic technologies in stem cell biology.
复制标题

DOI:
10.1016/j.chembiol.2021.02.001
复制
发表时间:
2021-03-18
影响因子:
8.6
通讯作者:
Chen S
Chen S
中科院分区:
生物学1区
文献类型:
--
作者:
Vandana JJ;Lacko LA;Chen S

文献摘要

参考文献

被引文献

相似文献

高通量表型筛选(HTPS)已成为发现调节干细胞命运的合成小分子的新兴技术。在这里,我们回顾了hTPS在识别控制干细胞更新、重编程、分化和谱系转换的小分子方面的应用。此外,我们还讨论了使用HTPS来发现模仿干细胞胞外利基的小分子/聚合物。此外,HTPSs已被应用于整个动物模型,以识别体内调节干细胞更新或分化的小分子。最后,我们讨论了HTPS在基于干细胞的疾病建模以及发现治疗癌症、糖尿病和传染病的新药候选方面的应用实例。总之,HTPS为干细胞领域提供了许多强大的工具,不仅促进了用于替代治疗、疾病建模和药物筛选的功能细胞/组织的产生,而且有助于剖析调节生理和病理过程的分子机制。Vandana等人。突出HTPS作为干细胞生物学中的强大工具的作用,以发现控制细胞规格和干细胞利基的小分子,扩大可用于疾病建模或治疗的新候选者的储存库。
The high-throughput phenotypic screen (HTPS) has become an emerging technology to discover synthetic small molecules that regulate stem cell fates. Here, we review the application of HTPS to identify small molecules controlling stem cell renewal, reprogramming, differentiation, and lineage conversion. Moreover, we discuss the use of HTPS to discover small molecules/polymers mimicking the stem cell extra-cellular niche. Furthermore, HTPSs have been applied on whole animal models to identify small molecules regulating stem cell renewal or differentiation in vivo. Finally, we discuss the examples of the utilization of HTPS in both stem cell-based disease modeling, as well as the discovery of novel drug candidates for cancer, diabetes, and infectious diseases. Overall, HTPSs have provided many powerful tools for the stem cell field, which not only facilitate the generation of functional cells/tissues for replacement therapy, disease modeling, and drug screening, but also help dissect molecular mechanisms regulating physiological and pathological processes. Vandana et al. highlight the role of HTPS as a powerful tool in stem cell biology to unearth small molecules that control cell specification and the stem cell niche, expanding the repository of novel candidates available for use in disease modeling or therapy.
DOI: 10.1002/adma.201501351
发表时间: 2015-07-15
期刊: Advanced materials (Deerfield Beach, Fla.)
影响因子: --
作者:
Celiz AD;Smith JG;Patel AK;Hook AL;Rajamohan D;George VT;Flatt L;Patel MJ;Epa VC;Singh T;Langer R;Anderson DG;Allen ND;Hay DC;Winkler DA;Barrett DA;Davies MC;Young LE;Denning C;Alexander MR
通讯作者: Alexander MR
DOI: 10.1016/j.stemcr.2016.12.004
发表时间: 2017-01-10
期刊: Stem cell reports
影响因子: 5.9
作者:
Astuti Y;Kramer AC;Blake AL;Blazar BR;Tolar J;Taisto ME;Lund TC
通讯作者: Lund TC
DOI: 10.1016/j.stem.2009.01.014
发表时间: 2009-04-03
期刊: Cell stem cell
影响因子: 23.9
作者:
Borowiak M;Maehr R;Chen S;Chen AE;Tang W;Fox JL;Schreiber SL;Melton DA
通讯作者: Melton DA
DOI: 10.1073/pnas.0608156103
发表时间: 2006-11-14
影响因子: 11.1
作者:
Chen, Shuibing;Do, Jeong Tae;Ding, Sheng
通讯作者: Ding, Sheng
DOI: 10.3390/molecules22122068
发表时间: 2017-11-27
期刊: Molecules (Basel, Switzerland)
影响因子: --
作者:
Chen JR;Lai YH;Tsai JJ;Hsiao CD
通讯作者: Hsiao CD