Massensini Andre R, Ghuman Harmanvir, Saldin Lindsey T, Medberry Christopher J, Keane Timothy J, Nicholls Francesca J, Velankar Sachin S, Badylak Stephen F, Modo Michel
University of Pittsburgh, McGowan Institute for Regenerative Medicine, Pittsburgh, PA, USA; University of Pittsburgh, Department of Radiology, Pittsburgh, PA, USA; Universidade Federal de Minas Gerais, Department of Physiology and Biophysics, Belo Horizonte, Brazil.
University of Pittsburgh, McGowan Institute for Regenerative Medicine, Pittsburgh, PA, USA; University of Pittsburgh, Department of Bioengineering, Pittsburgh, PA, USA.
Acta Biomater. 2015 Nov;27:116-130. doi: 10.1016/j.actbio.2015.08.040. Epub 2015 Aug 28.
Biomaterials composed of mammalian extracellular matrix (ECM) promote constructive tissue remodeling with minimal scar tissue formation in many anatomical sites. However, the optimal shape and form of ECM scaffold for each clinical application can vary markedly. ECM hydrogels have been shown to promote chemotaxis and differentiation of neuronal stem cells, but minimally invasive delivery of such scaffold materials to the central nervous system (CNS) would require an injectable form. These ECM materials can be manufactured to exist in fluid phase at room temperature, while forming hydrogels at body temperature in a concentration-dependent fashion. Implantation into the lesion cavity after a stroke could hence provide a means to support endogenous repair mechanisms. Herein, we characterize the rheological properties of an ECM hydrogel composed of urinary bladder matrix (UBM) that influence its delivery and in vivo interaction with host tissue. There was a notable concentration-dependence in viscosity, stiffness, and elasticity; all characteristics important for minimally invasive intracerebral delivery. An efficient MRI-guided injection with drainage of fluid from the cavity is described to assess in situ hydrogel formation and ECM retention at different concentrations (0, 1, 2, 3, 4, and 8mg/mL). Only ECM concentrations >3mg/mL gelled within the stroke cavity. Lower concentrations were not retained within the cavity, but extensive permeation of the liquid phase ECM into the peri-infarct area was evident. The concentration of ECM hydrogel is hence an important factor affecting gelation, host-biomaterial interface, as well intra-lesion distribution.
Extracellular matrix (ECM) hydrogel promotes constructive tissue remodeling in many tissues. Minimally invasive delivery of such scaffold materials to the central nervous system (CNS) would require an injectable form that exists in fluid phase at room temperature, while forming hydrogels at body temperature in a concentration-dependent fashion. We here report the rheological characterization of an injectable ECM hydrogel and its concentration-dependent delivery into a lesion cavity formed after a stroke based on MRI-guidance. The concentration of ECM determined its retention within the cavity or permeation into tissue and hence influenced its interaction with the host brain. This study demonstrates the importance of understanding the structure-function relationship of biomaterials to guide particular clinical applications.
由哺乳动物细胞外基质(ECM)组成的生物材料在许多解剖部位可促进建设性组织重塑,同时使瘢痕组织形成最少。然而,针对每种临床应用的ECM支架的最佳形状和形式可能有显著差异。已表明ECM水凝胶可促进神经干细胞的趋化性和分化,但将此类支架材料微创递送至中枢神经系统(CNS)需要可注射形式。这些ECM材料可制成在室温下呈液相存在,而在体温下以浓度依赖方式形成水凝胶。因此,中风后植入病变腔可为支持内源性修复机制提供一种手段。在此,我们表征了由膀胱基质(UBM)组成的ECM水凝胶的流变学特性,这些特性会影响其递送以及在体内与宿主组织的相互作用。在粘度、硬度和弹性方面存在显著的浓度依赖性;所有这些特性对于微创脑内递送都很重要。描述了一种有效的MRI引导注射以及从腔中引流液体,以评估不同浓度(0、1、2、3、4和8mg/mL)下原位水凝胶形成和ECM保留情况。仅ECM浓度>3mg/mL时在中风腔内形成凝胶。较低浓度未保留在腔内,但液相ECM广泛渗透到梗死周边区域是明显的。因此,ECM水凝胶的浓度是影响凝胶化、宿主 - 生物材料界面以及病变内分布的重要因素。
细胞外基质(ECM)水凝胶在许多组织中促进建设性组织重塑。将此类支架材料微创递送至中枢神经系统(CNS)需要一种可注射形式,该形式在室温下呈液相存在,而在体温下以浓度依赖方式形成水凝胶。我们在此报告了一种可注射ECM水凝胶的流变学表征及其在MRI引导下向中风后形成的病变腔内的浓度依赖性递送。ECM的浓度决定了其在腔内的保留或向组织的渗透,从而影响其与宿主脑的相互作用。本研究证明了理解生物材料的结构 - 功能关系以指导特定临床应用的重要性。