Menzies Health Institute Queensland, Griffith University, Southport, Queensland, Australia.
Clem Jones Centre for Neurobiology and Stem Cell Research, Griffith University, Brisbane, Queensland, Australia.
Cell Transplant. 2021 Jan-Dec;30:9636897211012909. doi: 10.1177/09636897211012909.
Cell transplantation shows promise for repair of the injured nervous system, including spinal cord injury (SCI) and peripheral nerve injury (PNI). There are, however, still problems hampering these therapies moving from bench to bedside, and the methods need optimization. Three-dimensional (3D) cell culture systems are suggested to improve outcomes, bridging the gap between the in vitro and in vivo environments. In such constructs, cells are allowed to interact with each other and with the extracellular matrix (ECM) in 3D as they do in vivo. Transplanting cells in 3D constructs, rather than in suspension, is thought to promote cell survival and maintain important cellular behaviors. One such critical behavior is cell migration into and within the injury site. Understanding and controlling the migratory capability of 3D-cultured cells is therefore pivotal for developing better transplantation techniques. ECM remodelling can influence numerous cellular functions, including cell migration and matrix metalloproteinases (MMPs) are important enzymes for ECM modulation. Here, we discuss the idea of modulating MMPs to control cell migration in 3D culture systems, which can improve the therapeutic potential of cells transplanted in 3D.
细胞移植显示出修复受损神经系统的潜力,包括脊髓损伤(SCI)和周围神经损伤(PNI)。然而,仍然存在一些问题阻碍了这些疗法从实验室走向临床,因此需要对这些方法进行优化。三维(3D)细胞培养系统被认为可以改善治疗效果,弥合体外和体内环境之间的差距。在这些构建体中,细胞可以像在体内一样相互作用,并与细胞外基质(ECM)在 3D 中相互作用。与悬浮培养相比,将细胞移植到 3D 构建体中被认为可以促进细胞存活并维持重要的细胞行为。其中一个关键行为是细胞迁移到损伤部位并在其中迁移。因此,了解和控制 3D 培养细胞的迁移能力对于开发更好的移植技术至关重要。细胞外基质重塑可以影响许多细胞功能,包括细胞迁移,而基质金属蛋白酶(MMPs)是细胞外基质调节的重要酶。在这里,我们讨论了通过调节 MMP 来控制 3D 培养系统中细胞迁移的想法,这可以提高在 3D 中移植的细胞的治疗潜力。