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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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