Lee Soah, Tong Xinming, Han Li-Hsin, Behn Anthony, Yang Fan
Department of Materials Science and Engineering, Stanford University, Stanford, California, 94305.
Department of Orthopaedic Surgery, Stanford University, Stanford, California, 94305.
J Biomed Mater Res A. 2016 May;104(5):1064-71. doi: 10.1002/jbm.a.35662. Epub 2016 Feb 14.
Smooth muscle tissue is characterized by aligned structures, which is critical for its contractile functions. Smooth muscle injury is common and can be caused by various diseases and degenerative processes, and there remains a strong need to develop effective therapies for smooth muscle tissue regeneration with restored structures. To guide cell alignment, previously cells were cultured on 2D nano/microgrooved substrates, but such method is limited to fabricating 2D aligned cell sheets only. Alternatively, aligned electrospun nanofiber has been employed as 3D scaffold for cell alignment, but cells can only be seeded post fabrication, and nanoporosity of electrospun fiber meshes often leads to poor cell distribution. To overcome these limitations, we report aligned gelatin-based microribbons (µRBs) as macroporous hydrogels for guiding smooth muscle alignment in 3D. We developed aligned µRB-like hydrogels using wet spinning, which allows easy fabrication of tissue-scale (cm) macroporous matrices with alignment cues and supports direct cell encapsulation. The macroporosity within µRB-based hydrogels facilitated cell proliferation, new matrix deposition, and nutrient diffusion. In aligned µRB scaffold, smooth muscle cells showed high viability, rapid adhesion, and alignment following µRB direction. Aligned µRB scaffolds supported retention of smooth muscle contractile phenotype, and accelerated uniaxial deposition of new matrix (collagen I/IV) along the µRB. In contrast, cells encapsulated in conventional gelatin hydrogels remained round with matrix deposition limited to pericellular regions only. We envision such aligned µRB scaffold can be broadly applicable in growing other anisotropic tissues including tendon, nerves and blood vessel.
平滑肌组织的特征在于其排列结构,这对其收缩功能至关重要。平滑肌损伤很常见,可由各种疾病和退行性过程引起,因此迫切需要开发有效的疗法来促进平滑肌组织再生并恢复其结构。为了引导细胞排列,此前细胞在二维纳米/微槽基底上培养,但这种方法仅限于制造二维排列的细胞片。另外,排列的电纺纳米纤维已被用作细胞排列的三维支架,但细胞只能在制造后接种,且电纺纤维网的纳米孔隙率常常导致细胞分布不佳。为克服这些限制,我们报道了排列的基于明胶的微带(µRBs)作为大孔水凝胶,用于在三维空间中引导平滑肌排列。我们通过湿法纺丝开发了排列的类µRB水凝胶,这使得能够轻松制造具有排列线索的组织尺度(厘米级)大孔基质,并支持直接细胞封装。基于µRB的水凝胶中的大孔隙促进了细胞增殖、新基质沉积和营养物质扩散。在排列的µRB支架中,平滑肌细胞显示出高活力、快速黏附,并沿µRB方向排列。排列的µRB支架支持平滑肌收缩表型的保留,并加速了新基质(胶原蛋白I/IV)沿µRB的单轴沉积。相比之下,封装在传统明胶水凝胶中的细胞保持圆形,基质沉积仅限于细胞周围区域。我们设想这种排列的µRB支架可广泛应用于培养包括肌腱、神经和血管在内的其他各向异性组织。