Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Tissue Eng Part A. 2022 Jul;28(13-14):640-650. doi: 10.1089/ten.TEA.2021.0161.
Transforming growth factor beta 2 (TGFβ2) is a pleiotropic growth factor that plays a vital role in smooth muscle cell (SMC) function. Our prior work has shown that SMC response can be modulated with TGFβ2 stimulation in a dose dependent manner. In particular, we have shown that increasing concentrations of TGFβ2 shift SMCs from a migratory to a synthetic behavior. In this work, electrospun compliance-matched and hypocompliant TGFβ2-eluting tissue engineered vascular grafts (TEVGs) were implanted into Sprague Dawley rats for 5 days to observe SMC population and collagen production. TEVGs were fabricated using a combined computational and experimental approach that varied the ratio of gelatin:polycaprolactone to be either compliance matched or twice as stiff as rat aorta (hypocompliant). TGFβ2 concentrations of 0, 10, 100 ng/mg were added to both graft types ( = 3 in each group) and imaged using ultrasound. Histological markers (SMC, macrophage, collagen, and elastin) were evaluated following explanation at 5 days. ultrasound showed that compliance-matched TEVGs became stiffer as TGFβ2 increased (100 ng/mg TEVGs compared to rat aorta, < 0.01), while all hypocompliant grafts remained stiffer than control rat aorta. velocity and diameter were also not significantly different than control vessels. The compliance-matched 10 ng/mg group had an elevated SMC signal (myosin heavy chain) compared to the 0 and 100 ng/mg grafts ( = 0.0009 and 0.0006). Compliance-matched TEVGs containing 100 ng/mg TGFβ2 had an increase in collagen production ( < 0.01), general immune response ( < 0.05), and a decrease in SMC population to the 0 and 10 ng/mg groups. All hypocompliant groups were found to be similar, suggesting a lower rate of TGFβ2 release in these TEVGs. Our results suggest that TGFβ2 can modulate SMC phenotype over an acute implantation period, which is consistent with our prior work. To the author's knowledge, this is the first rat study that evaluates a TGFβ2-eluting TEVG. Impact statement TGFβ2 affects the SMCs in a vascular graft.
转化生长因子β2(TGFβ2)是一种多功能生长因子,在平滑肌细胞(SMC)功能中起着至关重要的作用。我们之前的工作表明,SMC 反应可以通过 TGFβ2 刺激以剂量依赖的方式进行调节。特别是,我们已经表明,增加 TGFβ2 的浓度会使 SMC 从迁移行为转变为合成行为。在这项工作中,将顺应性匹配和低顺应性 TGFβ2 洗脱组织工程血管移植物(TEVG)植入 Sprague Dawley 大鼠体内 5 天,以观察 SMC 群体和胶原蛋白产生。TEVG 是使用结合计算和实验的方法制造的,改变明胶:聚己内酯的比例,使其顺应性匹配或比大鼠主动脉硬两倍(低顺应性)。将 0、10、100ng/mg 的 TGFβ2 浓度添加到两种移植物类型中(每组 3 个),并使用超声进行成像。在 5 天后解释后,评估组织学标记物(SMC、巨噬细胞、胶原蛋白和弹性蛋白)。超声显示,随着 TGFβ2 的增加,顺应性匹配的 TEVG 变得更硬(100ng/mg 的 TEVG 与大鼠主动脉相比, < 0.01),而所有低顺应性移植物仍比对照大鼠主动脉硬。速度和直径也与对照血管没有显著差异。与 0 和 100ng/mg 移植物相比,顺应性匹配的 10ng/mg 组的 SMC 信号(肌球蛋白重链)升高( = 0.0009 和 0.0006)。含有 100ng/mg TGFβ2 的顺应性匹配 TEVG 胶原产量增加( < 0.01),一般免疫反应增加( < 0.05),SMC 群体减少到 0 和 10ng/mg 组。所有低顺应性组均相似,表明这些 TEVG 中 TGFβ2 的释放速度较低。我们的结果表明,TGFβ2 可以在急性植入期间调节 SMC 表型,这与我们之前的工作一致。据作者所知,这是第一项评估 TGFβ2 洗脱 TEVG 的大鼠研究。影响说明 TGFβ2 影响血管移植物中的 SMC。