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首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Genetically engineered mesenchymal stem cell therapy using self-assembling supramolecular hydrogels
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Genetically engineered mesenchymal stem cell therapy using self-assembling supramolecular hydrogels

机译:自组装超分子水凝胶的基因工程间充质干细胞疗法

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Stem cell therapy has attracted a great deal of attention for treating intractable diseases such as cancer, stroke, liver cirrhosis, and ischemia. Especially, mesenchymal stemcells (MSCs) have been widely investigated for therapeutic applications due to the advantageous characteristics of long life-span, facile isolation, rapid proliferation, prolonged transgene expression, hypo-immunogenicity, and tumor tropism. MSCs can exert their therapeutic effects by releasing stress-induced therapeutic molecules after their rapid migration to damaged tissues. Recently, to improve the therapeutic efficacy, genetically engineered MSCs have been developed for therapeutic transgene expression by viral gene transduction and non-viral gene transfection. In general, the number of therapeutic cells for injection should be more than several millions for effective cell therapy. Adequate carriers for the controlled delivery of MSCs can reduce the required cell numbers and extend the duration of therapeutic effect, which provide great benefits for chronic disease patients. In this review, we describe genetic engineering of MSCs, recent progress of self-assembling supramolecular hydrogels, and their applications to cell therapy for intractable diseases and tissue regeneration. (C) 2015 Elsevier B.V. All rights reserved.
机译:干细胞疗法在治疗诸如癌症,中风,肝硬化和局部缺血等顽固性疾病方面引起了广泛的关注。特别地,由于长寿命,容易分离,快速增殖,延长的转基因表达,低免疫原性和肿瘤嗜性的优势特征,间充质干细胞(MSC)已被广泛研究用于治疗应用。 MSC可以通过在迅速迁移到受损组织后释放应力诱导的治疗分子来发挥治疗作用。最近,为了提高治疗效果,已经开发了基因工程的MSC,用于通过病毒基因转导和非病毒基因转染来表达治疗性转基因。通常,用于有效细胞治疗的注射治疗细胞数应超过数百万。用于MSC受控递送的足够载体可以减少所需的细胞数量并延长治疗效果的持续时间,这对慢性病患者提供了极大的好处。在这篇综述中,我们描述了MSC的基因工程,自组装超分子水凝胶的最新进展及其在难治性疾病和组织再生的细胞治疗中的应用。 (C)2015 Elsevier B.V.保留所有权利。

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