Yergeshov Abdulla, Zoughaib Mohamed, Dayob Kenana, Kamalov Marat, Luong Duong, Zakirova Albina, Mullin Ruslan, Salakhieva Diana, Abdullin Timur I
Scientific and Educational Center of Pharmaceutics, Kazan (Volga Region) Federal University, 18 Kremlyovskaya St., 420008 Kazan, Russia.
Institute of Fundamental Medicine and Biology, Kazan (Volga Region) Federal University, 18 Kremlyovskaya St., 420008 Kazan, Russia.
Pharmaceutics. 2024 Dec 8;16(12):1569. doi: 10.3390/pharmaceutics16121569.
The combination of macroporous cryogels with synthetic peptide factors represents a promising but poorly explored strategy for the development of extracellular matrix (ECM)-mimicking scaffolds for peripheral nerve (PN) repair. In this study, IKVAV peptide was functionalized with terminal lysine residues to allow its in situ cross-linking with gelatin macromer, resulting in the formation of IKVAV-containing proteinaceous cryogels. The controllable inclusion and distribution of the peptide molecules within the scaffold was verified using a fluorescently labelled peptide counterpart. The optimized cryogel scaffold was combined with polycaprolactone (PCL)-based shell tube to form a suturable nerve conduit (NC) to be implanted into sciatic nerve diastasis in rats. The NC constituents did not impair the viability of primary skin fibroblasts. Concentration-dependent effects of the peptide component on interrelated viscoelastic and swelling properties of the cryogels as well as on proliferation and morphological differentiation of neurogenic PC-12 cells were established, also indicating the existence of an optimal-density range of the introduced peptide. The in vivo implanted NC sustained the connection of the nerve stumps with partial degradation of the PCL tube over eight weeks, whereas the core-filling cryogel profoundly improved local electromyographic recovery and morphological repair of the nerve tissues, confirming the regenerative activity of the developed scaffold. These results provide proof-of-concept for the development of a newly designed PN conduit prototype based on IKVAV-activated cryogel, and they can be exploited to create other ECM-mimicking scaffolds.
大孔冷冻凝胶与合成肽因子相结合,是一种很有前景但尚未充分探索的策略,用于开发模仿细胞外基质(ECM)的支架,以修复周围神经(PN)。在本研究中,IKVAV肽通过末端赖氨酸残基进行功能化,以使其能够与明胶大分子原位交联,从而形成含IKVAV的蛋白质冷冻凝胶。使用荧光标记的肽类似物验证了肽分子在支架内的可控包封和分布。将优化后的冷冻凝胶支架与基于聚己内酯(PCL)的外壳管相结合,形成可缝合的神经导管(NC),植入大鼠坐骨神经间隙。NC成分不会损害原代皮肤成纤维细胞的活力。确定了肽成分对冷冻凝胶的相关粘弹性和溶胀特性以及对神经源性PC-12细胞增殖和形态分化的浓度依赖性影响,这也表明所引入肽存在最佳密度范围。体内植入的NC在八周内维持了神经断端的连接,同时PCL管部分降解,而核心填充的冷冻凝胶显著改善了局部肌电图恢复和神经组织的形态修复,证实了所开发支架的再生活性。这些结果为基于IKVAV激活的冷冻凝胶开发新设计的PN导管原型提供了概念验证,并且可用于创建其他模仿ECM的支架。