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Silk-Based Matrices and c-Kit-Positive Cardiac Progenitor Cells for a Cellularized Silk Fibroin Scaffold: Study of an in vivo Model

机译:用于细胞化丝素蛋白支架的丝基质和 c-KIT 阳性心脏祖细胞:体内模型的研究

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The production of a cellularized silk fibroin scaffold is very difficult because it is actually impossible to differentiate cells into a well-organized cardiac tissue. Without vascularization, not only do cell masses fail to grow, but they may also exhibit an area of necrosis, indicating a lack of oxygen and nutrients. In the present study, we used the so-called tyrosine protein kinase kit (c-Kit)-positive cardiac progenitor cells (CPCs) to generate cardiac cellularized silk fibroin scaffolds, multipotent cells isolated from the adult heart to date that can show some degree of differentiation toward the cardiac phenotype. To test their ability to differentiate into the cardiac phenotype in vivo as well, CPC and collagen organoid-like masses were implanted into nude mice and their behavior observed. Since the 3-dimensional structure of cardiac tissue can be preserved by scaffolds, we prepared in parallel different silk fibroin scaffolds with 3 different geometries and tested their behavior in 3 different models of immunosuppressed animals. Unfortunately, CPC cellularized silk fibroin scaffolds cannot be used in vivo. CPCs implanted alone or in collagen type I gel were destroyed by CD3+ lymphocyte aggregates, whereas the porous and partially oriented scaffolds elicited a consistent foreign body response characterized by giant cells. Only the electrospun meshes were resistant to the foreign body reaction. In conclusion, c-Kit-positive CPCs, although expressing a good level of cardiac differentiation markers in vitro with or without fibroin meshes, are not suitable for an in vivo model of cardiac organoids because they are degraded by a T-cell-mediated immune response. Even scaffolds which may preserve the survival of these cells in vivo also induced a host response. However, among the tested scaffolds, the electrospun meshes (F-scaffold) induced a lower response compared to all the other tested structures.
机译:细胞化丝素蛋白支架的生产非常困难,因为实际上不可能将细胞分化为组织良好的心脏组织。如果没有血管形成,细胞团不仅无法生长,而且还可能表现出坏死区域,表明缺乏氧气和营养。在本研究中,我们使用所谓的酪氨酸蛋白激酶试剂盒 (c-Kit) 阳性心脏祖细胞 (CPC) 来产生心脏细胞化丝素蛋白支架,这是迄今为止从成人心脏中分离出来的多能细胞,可以显示出一定程度的心脏表型分化。为了测试它们在体内分化为心脏表型的能力,将CPC和胶原类器官样肿块植入裸鼠中并观察它们的行为。由于心脏组织的三维结构可以通过支架保存,我们同时制备了具有 3 种不同几何形状的不同丝素蛋白支架,并在 3 种不同免疫抑制动物模型中测试了它们的行为。不幸的是,CPC细胞化丝素蛋白支架不能在体内使用。单独植入或植入 I 型胶原凝胶中的 CPC 被 CD3+ 淋巴细胞聚集体破坏,而多孔和部分取向的支架引发了以巨细胞为特征的一致异物反应。只有静电纺丝网对异物反应具有抵抗力。总之,c-Kit阳性CPC虽然在体外表达良好的心脏分化标志物水平,但无论是否使用丝心蛋白网,都不适合心脏类器官的体内模型,因为它们被T细胞介导的免疫反应降解。即使是可以在体内保存这些细胞存活的支架也诱导宿主反应。然而,在测试的支架中,与所有其他测试结构相比,静电纺丝网格(F-支架)诱导的响应较低。

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