Mauney Joshua R, Nguyen Trang, Gillen Kelly, Kirker-Head Carl, Gimble Jeffrey M, Kaplan David L
Department of Biomedical Engineering, Tufts University, 4 Colby Street, Medford, MA 02155, USA.
Biomaterials. 2007 Dec;28(35):5280-90. doi: 10.1016/j.biomaterials.2007.08.017. Epub 2007 Aug 31.
Biomaterials derived from silk fibroin prepared by aqueous (AB) and organic (HFIP) solvent-based processes, along with collagen (COL) and poly-lactic acid (PLA)-based scaffolds were studied in vitro and in vivo for their utility in adipose tissue engineering strategies. For in vitro studies, human bone marrow and adipose-derived mesenchymal stem cells (hMSCs and hASCs) were seeded on the various biomaterials and cultured for 21 days in the presence of adipogenic stimulants (AD) or maintained as noninduced controls. Alamar Blue analysis revealed each biomaterial supported initial attachment of hMSCs and hASCs to similar levels for all matrices except COL in which higher levels were observed. hASCs and hMSCs cultured on all biomaterials in the presence of AD showed significant upregulation of adipogenic mRNA transcript levels (LPL, GLUT4, FABP4, PPARgamma, adipsin, ACS) to similar extents when compared to noninduced controls. Similarly Oil-Red O analysis of hASC or hMSC-seeded scaffolds displayed substantial amounts of lipid accumulating adipocytes following cultivation with AD. The data revealed AB and HFIP scaffolds supported similar extents of lipid accumulating cells while PLA and COL scaffolds qualitatively displayed lower and higher extents by comparison, respectively. Following a 4-week implantation period in a rat muscle pouch defect model, both AB and HFIP scaffolds supported in vivo adipogenesis either alone or seeded with hASCs or hMSCs as assessed by Oil-Red O analysis, however the presence of exogenous cell sources substantially increased the extent and frequency of adipogenesis observed. In contrast, COL and PLA scaffolds underwent rapid scaffold degradation and were irretrievable following the implantation period. The results suggest that macroporous 3D AB and HFIP silk fibroin scaffolds offer an important platform for cell-based adipose tissue engineering applications, and in particular, provide longer-term structural integrity to promote the maintenance of soft tissue in vivo.
对通过水相(AB)和基于有机(六氟异丙醇,HFIP)溶剂的工艺制备的丝素蛋白衍生生物材料,以及胶原蛋白(COL)和聚乳酸(PLA)基支架进行了体内外研究,以探讨它们在脂肪组织工程策略中的效用。在体外研究中,将人骨髓和脂肪来源的间充质干细胞(hMSC和hASC)接种在各种生物材料上,并在脂肪生成刺激剂(AD)存在下培养21天,或作为未诱导对照进行培养。alamar Blue分析显示,除COL外,所有基质上的每种生物材料对hMSC和hASC的初始附着支持水平相似,而在COL上观察到更高的附着水平。与未诱导对照相比,在AD存在下于所有生物材料上培养的hASC和hMSC显示脂肪生成mRNA转录水平(脂蛋白脂肪酶,LPL、葡萄糖转运蛋白4,GLUT4、脂肪酸结合蛋白4,FABP4、过氧化物酶体增殖物激活受体γ,PPARγ、脂肪酶、酰基辅酶A合成酶,ACS)显著上调,且上调程度相似。同样,对接种hASC或hMSC的支架进行油红O分析显示,在用AD培养后,有大量脂质积累的脂肪细胞。数据显示,AB和HFIP支架支持的脂质积累细胞程度相似,而PLA和COL支架相比之下分别定性地显示出较低和较高的程度。在大鼠肌肉袋缺损模型中植入4周后,通过油红O分析评估,AB和HFIP支架单独或接种hASC或hMSC均支持体内脂肪生成,然而外源性细胞来源的存在显著增加了观察到的脂肪生成程度和频率。相比之下,COL和PLA支架在植入期后迅速降解且无法恢复。结果表明,大孔三维AB和HFIP丝素蛋白支架为基于细胞的脂肪组织工程应用提供了一个重要平台,特别是能提供长期的结构完整性,以促进体内软组织的维持。