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首页> 外文期刊>Biomaterials >Therapeutic angiogenesis by a myoblast layer harvested by tissue transfer printing from cell-adhesive, thermosensitive hydrogels
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Therapeutic angiogenesis by a myoblast layer harvested by tissue transfer printing from cell-adhesive, thermosensitive hydrogels

机译:通过从细胞粘附性热敏性水凝胶进行组织转移印刷收获的成肌细胞层进行治疗性血管生成

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摘要

Peripheral arterial disease (PAD) is characterized by the altered structure and function of arteries caused by accumulated plaque. There have been many studies on treating this disease by the direct injection of various types of therapeutic cells, however, the low cell engraftment efficiency and diffusion of the transplanted cells have been major problems. In this study, we developed an approach (transfer printing) to deliver monolayer of cells to the hindlimb ischemic tissue using thermosensitive hydrogels, and investigated its efficacy in long term retention upon transplantation and therapeutic angiogenesis. We first investigated the invitro maintenance of robust cell-cell contacts and stable expression of the ECM proteins in myoblast layer following transfer printing process. In order to confirm the therapeutic effect of the myoblasts invivo, we cultured a monolayer of C2C12 myoblasts on thermosensitive hydrogels, which was then transferred to the hindlimb ischemia tissue of athymic mice directly from the hydrogel by conformal contact. The transferred myoblast layer was retained for a longer period of time than an intramuscularly injected cell suspension. In addition, the morphology of the mice and laser Doppler perfusion (28 days after treatment) supported that the myoblast layer enhanced the therapeutic effects on the ischemic tissue. In summary, the transplantation of the C2C12 myoblast layer using a tissue transfer printing method could represent a new approach for the treatment of PAD by therapeutic angiogenesis.
机译:周围动脉疾病(PAD)的特征是由斑块累积引起的动脉结构和功能改变。通过直接注射各种类型的治疗细胞来治疗该疾病已有许多研究,但是,低的细胞植入效率和移植细胞的扩散已成为主要问题。在这项研究中,我们开发了一种使用热敏性水凝胶将细胞单层递送至后肢缺血组织的方法(转移印刷),并研究了其在移植和治疗性血管生成中长期保留的功效。我们首先研究了转染后在成肌细胞层中细胞与细胞之间的牢固接触以及ECM蛋白的稳定表达。为了确认成肌细胞在体内的治疗效果,我们在热敏水凝胶上培养了单层C2C12成肌细胞,然后通过保形接触将其直接从水凝胶转移到无胸腺小鼠的后肢缺血组织中。与肌内注射的细胞悬浮液相比,转移的成肌细胞层可以保留更长的时间。此外,小鼠的形态和激光多普勒灌注(治疗后28天)支持成肌细胞层增强了对缺血组织的治疗作用。总之,使用组织转移印刷方法移植C2C12成肌细胞层可能代表了一种通过治疗性血管生成治疗PAD的新方法。

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