Guiding Mesenchymal Stem Cells into Myelinating Schwann Cell-Like Phenotypes by Using Electrospun Core-Sheath Nanoyarns

被引:24
|
作者
Wu, Shaohua [1 ,4 ,5 ]
Ni, Shilei [6 ,7 ]
Jiang, Xiping [1 ]
Kuss, Mitchell A. [1 ]
Wang, Han-Jun [2 ]
Duan, Bin [1 ,3 ,8 ]
机构
[1] Univ Nebraska Med Ctr, Coll Med, Mary & Dick Holland Regenerat Med Program, Div Cardiol,Dept Internal Med, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Dept Anesthesiol, Coll Med, Omaha, NE 68198 USA
[3] Univ Nebraska Med Ctr, Dept Surg, Coll Med, Omaha, NE 68198 USA
[4] Qingdao Univ, Coll Text & Clothing, Qingdao 266071, Shandong, Peoples R China
[5] Qingdao Univ, Collaborat Innovat Ctr Marine Biomass Fibers, Qingdao 266071, Shandong, Peoples R China
[6] Shandong Univ, Qilu Hosp, Dept Neurosurg, Jinan 250012, Shandong, Peoples R China
[7] Shandong Univ, Inst Brain & Brain Inspired Sci, Jinan 250012, Shandong, Peoples R China
[8] Univ Nebraska, Dept Mech & Mat Engn, Lincoln, NE 68588 USA
来源
基金
美国国家卫生研究院;
关键词
core sheath yarn; myelination; Schwann cell-like differentiation; cell migration; nerve regeneration; PERIPHERAL-NERVE REGENERATION; NEURITE OUTGROWTH; FUNCTIONAL RECOVERY; GUIDANCE CONDUIT; SPINAL-CORD; DIFFERENTIATION; PROMOTE; HYDROGEL; INJURY; NANOFIBERS;
D O I
10.1021/acsbiomaterials.9b00748
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Nerve guidance conduit (NGC)-infilling substrates have been reported to facilitate the regeneration of injured peripheral nerves (PNs), especially for large nerve gaps. In this study, longitudinally oriented electrospun core-sheath nanoyarns (csNYs), consisting of a polylactic acid microfiber core and an electrospun nanofiber sheath, were fabricated for potential PN tissue engineering applications. Our novel csNY displayed a well-aligned nanofibrous surface topography, resembling the ultrastructure of axons and fascicles of a native PN system, and it also provided a mechanically stable structure. The biological results showed that the csNY significantly enhanced the attachment, growth, and proliferation of human adipose derived mesenchymal stem cells (hADMSC) and also promoted the migration, proliferation, and phenotype maintenance of rabbit Schwann cells (rSCs). Our csNY notably increased the differentiation capability of hADMSC into SC-like cells (hADMSC-SC), in comparison with a 2D tissue culture polystyrene plate. More importantly, when combined with the appropriate induction medium, our csNY promoted hADMSC-SC to express high levels of myelination-associated markers. Overall, this study demonstrates that our csNYs have great potential to serve as not only ideal in vitro culture models for understanding SC-axon interaction and SC myelination but also as promising NGC-infilling substrates for PN regeneration applications.
引用
收藏
页码:5284 / 5294
页数:21
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