Kasyanov Vladimir A, Hodde Jason, Hiles Michael C, Eisenberg Carol, Eisenberg Leonard, De Castro Luis E F, Ozolanta Iveta, Murovska Modra, Draughn Robert A, Prestwich Glenn D, Markwald Roger R, Mironov Vladimir
Medical University of South Carolina, Charleston, SC 29426, USA.
J Mater Sci Mater Med. 2009 Jan;20(1):329-37. doi: 10.1007/s10856-008-3590-3. Epub 2008 Sep 20.
Centrifugal casting allows rapid biofabrication of tubular tissue constructs by suspending living cells in an in situ cross-linkable hydrogel. We hypothesize that introduction of laser-machined micropores into a decellularized natural scaffold will facilitate cell seeding by centrifugal casting and increase hydrogel retention, without compromising the biomechanical properties of the scaffold. Micropores with diameters of 50, 100, and 200 mum were machined at different linear densities in decellularized small intestine submucosa (SIS) planar sheets and tubular SIS scaffolds using an argon laser. The ultimate stress and ultimate strain values for SIS sheets with laser-machined micropores with diameter 50 mum and distance between holes as low as 714 mum were not significantly different from unmachined control SIS specimens. Centrifugal casting of GFP-labeled cells suspended in an in situ cross-linkable hyaluronan-based hydrogel resulted in scaffold recellularization with a high density of viable cells inside the laser-machined micropores. Perfusion tests demonstrated the retention of the cells encapsulated within the HA hydrogel in the microholes. Thus, an SIS scaffold with appropriately sized microholes can be loaded with hydrogel encapsulated cells by centrifugal casting to give a mechanically robust construct that retains the cell-seeded hydrogel, permitting rapid biofabrication of tubular tissue construct in a "bioreactor-free" fashion.
离心铸造法可通过将活细胞悬浮于原位可交联水凝胶中来快速生物制造管状组织构建体。我们推测,在脱细胞天然支架中引入激光加工的微孔将有助于通过离心铸造进行细胞接种,并增加水凝胶的保留率,同时不损害支架的生物力学性能。使用氩激光在脱细胞小肠黏膜下层(SIS)平面片材和管状SIS支架中以不同的线密度加工直径为50、100和200μm的微孔。直径为50μm且孔间距低至714μm的带有激光加工微孔的SIS片材的极限应力和极限应变值与未加工的对照SIS标本无显著差异。将悬浮于原位可交联透明质酸基水凝胶中的绿色荧光蛋白标记细胞进行离心铸造,导致支架重新细胞化,激光加工微孔内有高密度的活细胞。灌注试验证明了包裹在HA水凝胶中的细胞在微孔中的保留。因此,具有适当尺寸微孔的SIS支架可通过离心铸造加载水凝胶包裹的细胞,从而得到一种机械坚固的构建体,该构建体保留了接种细胞的水凝胶,允许以“无生物反应器”的方式快速生物制造管状组织构建体。