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Targeted Treatment of Ischemic and Fibrotic Complications of Myocardial Infarction Using a Dual-Delivery Microgel Therapeutic.采用双载药微凝胶治疗策略靶向治疗心肌梗死的缺血性和纤维化并发症。
ACS Nano. 2018 Aug 28;12(8):7826-7837. doi: 10.1021/acsnano.8b01977. Epub 2018 Jul 25.
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Injectable and protease-degradable hydrogel for siRNA sequestration and triggered delivery to the heart.用于 siRNA 隔离和触发递送至心脏的可注射和蛋白酶可降解水凝胶。
J Control Release. 2018 Sep 10;285:152-161. doi: 10.1016/j.jconrel.2018.07.004. Epub 2018 Jul 4.
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Characterization and Validation of a Human 3D Cardiac Microtissue for the Assessment of Changes in Cardiac Pathology.用于评估心脏病理学变化的人类 3D 心脏微组织的特征描述和验证。
Sci Rep. 2018 Jul 5;8(1):10160. doi: 10.1038/s41598-018-28393-y.
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Generation of spatial-patterned early-developing cardiac organoids using human pluripotent stem cells.使用人类多能干细胞生成具有空间图案的早期心脏类器官。
Nat Protoc. 2018 Apr;13(4):723-737. doi: 10.1038/nprot.2018.006. Epub 2018 Mar 15.
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Modeling human diseases with induced pluripotent stem cells: from 2D to 3D and beyond.利用诱导多能干细胞模拟人类疾病:从二维到三维及更深入发展
Development. 2018 Mar 8;145(5):dev156166. doi: 10.1242/dev.156166.
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Force Generation via β-Cardiac Myosin, Titin, and α-Actinin Drives Cardiac Sarcomere Assembly from Cell-Matrix Adhesions.通过β-心脏肌球蛋白、肌联蛋白和α-辅肌动蛋白产生的力驱动细胞-基质黏附处的心肌肌节组装。
Dev Cell. 2018 Jan 8;44(1):87-96.e5. doi: 10.1016/j.devcel.2017.12.012.
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Cardiopatch platform enables maturation and scale-up of human pluripotent stem cell-derived engineered heart tissues.心脏贴片平台可实现人类多能干细胞衍生的工程心脏组织的成熟和规模化。
Nat Commun. 2017 Nov 28;8(1):1825. doi: 10.1038/s41467-017-01946-x.
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Functional screening in human cardiac organoids reveals a metabolic mechanism for cardiomyocyte cell cycle arrest.人类心脏类器官中的功能筛选揭示了心肌细胞细胞周期停滞的代谢机制。
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9
A 3D magnetic tissue stretcher for remote mechanical control of embryonic stem cell differentiation.一种用于远程机械控制胚胎干细胞分化的 3D 磁性组织拉伸器。
Nat Commun. 2017 Sep 12;8(1):400. doi: 10.1038/s41467-017-00543-2.
10
Effect of shear stress on iPSC-derived human brain microvascular endothelial cells (dhBMECs).切应力对诱导多能干细胞源性人脑微血管内皮细胞(dhBMECs)的影响。
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机械因素对心血管分化和疾病建模的影响。

Mechanical influences on cardiovascular differentiation and disease modeling.

机构信息

Department of Bioengineering, University of California, San Diego, La Jolla, CA 92093, United States; Sanford Consortium for Regenerative Medicine, La Jolla, CA 92037, United States.

Department of Bioengineering, University of California, San Diego, La Jolla, CA 92093, United States; Sanford Consortium for Regenerative Medicine, La Jolla, CA 92037, United States.

出版信息

Exp Cell Res. 2019 Apr 15;377(1-2):103-108. doi: 10.1016/j.yexcr.2019.02.019. Epub 2019 Feb 19.

DOI:10.1016/j.yexcr.2019.02.019
PMID:30794804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6408970/
Abstract

Tissues are continuously exposed to forces in vivo, whether from fluid pressure in an artery from our blood or compressive forces on joints from our body weight. The forces that cells are exposed to arise almost immediately after conception; it is therefore important to understand how forces shape stem cell differentiation into lineage committed cells, how they help organize cells into tissues, and how forces can cause or exacerbate disease. No tissue is exempt, but cardiovascular tissues in particular are exposed to these forces. While animal models have been used extensively in the past, there is growing recognition of their limitations when modeling disease complexity or human genetics. In this mini review, we summarize current understanding of the mechanical influences on the differentiation of cardiovascular progeny, how the transduction of forces influence the onset of disease, and how engineering approaches applied to this problem have yielded systems that create mature-like human tissues in vitro in which to assess the impact of disease on cell function.

摘要

组织在体内不断受到力的作用,无论是来自血液中动脉的流体压力,还是来自我们体重的关节压缩力。细胞所承受的力几乎是在受孕后立即产生的;因此,了解力如何塑造干细胞分化为谱系定向细胞,帮助组织中的细胞如何组织起来,以及力如何导致或加剧疾病,这一点非常重要。没有组织可以豁免,但心血管组织尤其容易受到这些力的影响。虽然过去广泛使用了动物模型,但人们越来越认识到它们在模拟疾病复杂性或人类遗传学方面的局限性。在这篇迷你综述中,我们总结了目前对心血管祖细胞分化的机械影响的理解,力的转导如何影响疾病的发生,以及应用于该问题的工程方法如何产生了类似于成熟的人类组织的体外系统,可用于评估疾病对细胞功能的影响。