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用于心血管组织工程的基于凝集素和抗体的组织化学技术。

Lectin and antibody-based histochemical techniques for cardiovascular tissue engineering.

作者信息

Simionescu Agneta, Tedder Mary E, Chuang Ting-Hsien, Simionescu Dan T

机构信息

Department of Bioengineering, Clemson University, Clemson, SC, USA.

出版信息

J Histotechnol. 2011 Mar;34(1):20-28. doi: 10.1179/014788811X12949268296040.

Abstract

Tissue engineering holds immense potential for treatment of cardiovascular diseases by creating living structures to replace diseased blood vessels, heart valves, and cardiac muscle. In a traditional approach, scaffolds are seeded with stem cells and subjected to stimuli in bioreactors that mimic physiologic conditions or are directly implanted into target sites in animal models. The expected results are significant cell changes, extensive remodeling of the scaffolds and creation of surrogate structures that would be deemed acceptable for tissue regeneration. Histochemical techniques are increasingly becoming essential tools in tissue engineering research. In our studies, we used lectin and antibody-based techniques to characterize novel collagen and elastin scaffolds and to ensure efficient removal of xenoantigens. Scaffolds were implanted in animals and infiltrated host cells were identified using antibodies to activated fibroblasts, macrophages, and lymphocytes. Stem cell-seeded scaffolds were subjected to mechanical strains and tested for differentiation into cardiovascular cells using antibody-based double immunofluorescence methods. Finally, living heart valves were constructed from scaffolds and stem cells, subjected to conditioning in a bioreactor and stem cell differentiation evaluated by immunofluorescence. Overall, these techniques have proven to be outstanding companions to biochemical, molecular biology and cell analysis methods used in tissue engineering research and development.

摘要

组织工程通过构建活体结构来替代病变的血管、心脏瓣膜和心肌,在心血管疾病治疗方面具有巨大潜力。在传统方法中,将干细胞接种到支架上,并在模拟生理条件的生物反应器中对其施加刺激,或者直接将其植入动物模型的靶位点。预期结果是细胞发生显著变化、支架进行广泛重塑以及生成被认为可用于组织再生的替代结构。组织化学技术正日益成为组织工程研究中的重要工具。在我们的研究中,我们使用基于凝集素和抗体的技术来表征新型胶原蛋白和弹性蛋白支架,并确保有效去除异种抗原。将支架植入动物体内,使用针对活化成纤维细胞、巨噬细胞和淋巴细胞的抗体来识别浸润的宿主细胞。对接种了干细胞的支架施加机械应变,并使用基于抗体的双重免疫荧光方法检测其向心血管细胞的分化情况。最后,用支架和干细胞构建活体心脏瓣膜,在生物反应器中进行预处理,并通过免疫荧光评估干细胞的分化情况。总体而言,这些技术已被证明是组织工程研发中使用的生化、分子生物学和细胞分析方法的出色辅助手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c09/4303246/68bc7749cbe8/nihms-653128-f0001.jpg

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