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在水凝胶中递送脑源性神经营养因子的药理活性微载体:用于人骨髓源干细胞神经/神经元分化引导及治疗性分泌组增强的新策略。

Pharmacologically active microcarriers delivering BDNF within a hydrogel: Novel strategy for human bone marrow-derived stem cells neural/neuronal differentiation guidance and therapeutic secretome enhancement.

作者信息

Kandalam Saikrishna, Sindji Laurence, Delcroix Gaëtan J-R, Violet Fabien, Garric Xavier, André Emilie M, Schiller Paul C, Venier-Julienne Marie-Claire, des Rieux Anne, Guicheux Jérôme, Montero-Menei Claudia N

机构信息

INSERM U 1066, 'Micro et Nanomédecines biomimétiques-MINT', Angers, France; Université Angers, UMR-S1066, Angers, France.

GRECC and Research Service, Veterans Affairs Medical Center, Miami, FL, USA; Department of Orthopaedics, University of Miami Miller School of Medicine, FL, USA; Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

Acta Biomater. 2017 Feb;49:167-180. doi: 10.1016/j.actbio.2016.11.030. Epub 2016 Nov 16.


DOI:10.1016/j.actbio.2016.11.030
PMID:27865962
Abstract

UNLABELLED: Stem cells combined with biodegradable injectable scaffolds releasing growth factors hold great promises in regenerative medicine, particularly in the treatment of neurological disorders. We here integrated human marrow-isolated adult multilineage-inducible (MIAMI) stem cells and pharmacologically active microcarriers (PAMs) into an injectable non-toxic silanized-hydroxypropyl methylcellulose (Si-HPMC) hydrogel. The goal is to obtain an injectable non-toxic cell and growth factor delivery device. It should direct the survival and/or neuronal differentiation of the grafted cells, to safely transplant them in the central nervous system, and enhance their tissue repair properties. A model protein was used to optimize the nanoprecipitation conditions of the neuroprotective brain-derived neurotrophic factor (BDNF). BDNF nanoprecipitate was encapsulated in fibronectin-coated (FN) PAMs and the in vitro release profile evaluated. It showed a prolonged, bi-phasic, release of bioactive BDNF, without burst effect. We demonstrated that PAMs and the Si-HPMC hydrogel increased the expression of neural/neuronal differentiation markers of MIAMI cells after 1week. Moreover, the 3D environment (PAMs or hydrogel) increased MIAMI cells secretion of growth factors (b-NGF, SCF, HGF, LIF, PlGF-1, SDF-1α, VEGF-A & D) and chemokines (MIP-1α & β, RANTES, IL-8). These results show that PAMs delivering BDNF combined with Si-HPMC hydrogel represent a useful novel local delivery tool in the context of neurological disorders. It not only provides neuroprotective BDNF but also bone marrow-derived stem cells that benefit from that environment by displaying neural commitment and an improved neuroprotective/reparative secretome. It provides preliminary evidence of a promising pro-angiogenic, neuroprotective and axonal growth-promoting device for the nervous system. STATEMENT OF SIGNIFICANCE: Combinatorial tissue engineering strategies for the central nervous system are scarce. We developed and characterized a novel injectable non-toxic stem cell and protein delivery system providing regenerative cues for central nervous system disorders. BDNF, a neurotrophic factor with a wide-range effect, was nanoprecipitated to maintain its structure and released in a sustained manner from novel polymeric microcarriers. The combinatorial 3D support, provided by fibronectin-microcarriers and the hydrogel, to the mesenchymal stem cells guided the cells towards a neuronal differentiation and enhanced their tissue repair properties by promoting growth factors and cytokine secretion. The long-term release of physiological doses of bioactive BDNF, combined to the enhanced secretion of tissue repair factors from the stem cells, constitute a promising therapeutic approach.

摘要

未标记:干细胞与可释放生长因子的可生物降解注射支架相结合,在再生医学领域,尤其是在神经系统疾病的治疗中具有巨大潜力。我们在此将人骨髓分离的成年多谱系诱导(MIAMI)干细胞和具有药理活性的微载体(PAM)整合到一种可注射的无毒硅烷化羟丙基甲基纤维素(Si-HPMC)水凝胶中。目标是获得一种可注射的无毒细胞和生长因子递送装置。它应引导移植细胞的存活和/或神经元分化,将它们安全地移植到中枢神经系统中,并增强其组织修复特性。使用一种模型蛋白来优化神经保护因子脑源性神经营养因子(BDNF)的纳米沉淀条件。将BDNF纳米沉淀物包裹在纤连蛋白包被(FN)的PAM中,并评估其体外释放曲线。结果显示,生物活性BDNF呈现出延长的双相释放,无突释效应。我们证明,PAM和Si-HPMC水凝胶在1周后增加了MIAMI细胞神经/神经元分化标志物的表达。此外,三维环境(PAM或水凝胶)增加了MIAMI细胞生长因子(b-NGF、SCF、HGF、LIF、PlGF-1、SDF-1α、VEGF-A和D)和趋化因子(MIP-1α和β、RANTES、IL-8)的分泌。这些结果表明,递送BDNF的PAM与Si-HPMC水凝胶相结合,在神经系统疾病的背景下是一种有用的新型局部递送工具。它不仅提供神经保护因子BDNF,还提供骨髓来源的干细胞,这些干细胞通过表现出神经定向和改善的神经保护/修复分泌组而从该环境中受益。它为一种有前景的促进血管生成、神经保护和轴突生长的神经系统装置提供了初步证据。 意义声明:用于中枢神经系统的组合组织工程策略很少。我们开发并表征了一种新型的可注射无毒干细胞和蛋白质递送系统,为中枢神经系统疾病提供再生线索。BDNF是一种具有广泛作用的神经营养因子,通过纳米沉淀来维持其结构,并从新型聚合物微载体中持续释放。纤连蛋白微载体和水凝胶提供的组合三维支持,引导间充质干细胞向神经元分化,并通过促进生长因子和细胞因子的分泌来增强其组织修复特性。生理剂量生物活性BDNF的长期释放,与干细胞组织修复因子分泌的增强相结合,构成了一种有前景的治疗方法。

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