Human cells can not grow into tissues without a scaffold or extra-cellular matrix to attach to. This limits the ability of damaged tissue to heal after injury or disease. Recently, researchers at Nanyang Technical University used PCL (AP257, AP260) and PLA (AP047, AP114) from PolySciTech (www.polyscitech.com) to create nanofiber meshes and evaluate their effect on myelination. This research holds promise to provide for improved treatment of damage in the central nervous system by providing a scaffold for cells to grow on. Read more: Ong, William, Nicolas Marinval, Junquan Lin, Mui Hoon Nai, Yee‐Song Chong, Coline Pinese, Sreedharan Sajikumar et al. "Biomimicking Fiber Platform with Tunable Stiffness to Study Mechanotransduction Reveals Stiffness Enhances Oligodendrocyte Differentiation but Impedes Myelination through YAP‐Dependent Regulation." Small (2020): 2003656. https://onlinelibrary.wiley.com/doi/abs/10.1002/smll.202003656
“A key hallmark of many diseases, especially those in the central nervous system (CNS), is the change in tissue stiffness due to inflammation and scarring. However, how such changes in microenvironment affect the regenerative process remains poorly understood. Here, a biomimicking fiber platform that provides independent variation of fiber structural and intrinsic stiffness is reported. To demonstrate the functionality of these constructs as a mechanotransduction study platform, these substrates are utilized as artificial axons and the effects of axon structural versus intrinsic stiffness on CNS myelination are independently analyzed. While studies have shown that substrate stiffness affects oligodendrocyte differentiation, the effects of mechanical stiffness on the final functional state of oligodendrocyte (i.e., myelination) has not been shown prior to this. Here, it is demonstrated that a stiff mechanical microenvironment impedes oligodendrocyte myelination, independently and distinctively from oligodendrocyte differentiation. Yes‐associated protein is identified to be involved in influencing oligodendrocyte myelination through mechanotransduction. The opposing effects on oligodendrocyte differentiation and myelination provide important implications for current work screening for promyelinating drugs, since these efforts have focused mainly on promoting oligodendrocyte differentiation. Thus, the platform may have considerable utility as part of a drug discovery program in identifying molecules that promote both differentiation and myelination.”
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