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Transplantation of layer-by-layer assembled neural stem cells tethered with vascular endothelial growth factor reservoir promotes neurogenesis and angiogenesis after ischemic stroke in mice AITranslate

Third Military Medical University (Army Medical University); Affiliated Hospital of Zunyi Medical University; Third Military Medical University (Army Medical University); School of Medicine of Anhui Medical University; Third Military Medical University (Army Medical University); Third Military Medical University (Army Medical University); Third Military Medical University (Army Medical University); Affiliated Hospital of Zunyi Medical University; Affiliated Hospital of Zunyi Medical University; Affiliated Hospital of Zunyi Medical University; Third Military Medical University (Army Medical University); Third Military Medical University (Army Medical University); Third Military Medical University (Army Medical University)
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Publisher: Elsevier
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Abstract AITranslate

Transplantation of neural stem cells (NSCs) is a promising therapeutic strategy for ischemic stroke. However, most of engrafted NSCs hardly survive for a long time, and the majority of transplanted NSCs differentiate into astrocytes around infarct core due to harsh microenvironment after ischemic stroke. Therefore, exploring approaches to foster the regenerative ability of transplanted NSCs in hostile niche is a feasible strategy to rehabilitate lesions. Here, a feasible method for grafted NSCs modified by layer-by-layer (LbL) assembly (LbL-NSCs) using gelatin and hyaluronic acid (HA) was developed. The results indicated the LbL-NSCs were biocompatible, and held the ability of promoting NSCs differentiation into neurons. Subsequently, vascular endothelial growth factor (VEGF) was laden into gelatin to generate LbL-NSCs tethered with VEGF reservoir [LbL (VEGF)-NSCs], and the VEGF releasing from LbL (VEGF)-NSCs was sustained under pH 7.4 in vitro. Afterward, the results demonstrated transplantation of LbL (VEGF)-NSCs facilitated implanted NSCs survival and differentiation into neurons in distal middle cerebral artery occlusion (dMCAO) mice. Additionally, engraftment of LbL (VEGF)-NSCs reinforced neurogenesis, angiogenesis, survival of host neurons, and blood brain barrier (BBB) repair, thereafter enhancing functional recovery through reducing the volume of infarct core in dMCAO mice. This investigation provides an appropriate approach for modifying NSCs by LbL assembly using gelatin loaded with VEGF and HA to expedite the rehabilitative ability of engrafted NSCs following ischemic stroke. Graphical abstract Graphical illustration of the fabrication of layer-by-layer (LbL) assembled NSCs tethered with VEGF reservoir [LbL (VEGF)-NSCs], and therapeutic effects of LbL (VEGF)-NSCs on neurovascular network rehabilitation after transplantation in mice with ischemic stroke. Download : Download high-res image (221KB) Download : Download full-size image

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DOI:https://doi.org/10.1016/j.apmt.2022.101548

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Citation Information:

Transplantation of neural stem cells (NSCs) is a promising therapeutic strategy for ischemic stroke. However, most of engrafted NSCs hardly survive for a long time, and the majority of transplanted NSCs differentiate into astrocytes around infarct core due to harsh microenvironment after ischemic stroke. Therefore, exploring approaches to foster the regenerative ability of transplanted NSCs in hostile niche is a feasible strategy to rehabilitate lesions. Here, a feasible method for grafted NSCs modified by layer-by-layer (LbL) assembly (LbL-NSCs) using gelatin and hyaluronic acid (HA) was developed. The results indicated the LbL-NSCs were biocompatible, and held the ability of promoting NSCs differentiation into neurons. Subsequently, vascular endothelial growth factor (VEGF) was laden into gelatin to generate LbL-NSCs tethered with VEGF reservoir [LbL (VEGF)-NSCs], and the VEGF releasing from LbL (VEGF)-NSCs was sustained under pH 7.4 in vitro. Afterward, the results demonstrated transplantation of LbL (VEGF)-NSCs facilitated implanted NSCs survival and differentiation into neurons in distal middle cerebral artery occlusion (dMCAO) mice. Additionally, engraftment of LbL (VEGF)-NSCs reinforced neurogenesis, angiogenesis, survival of host neurons, and blood brain barrier (BBB) repair, thereafter enhancing functional recovery through reducing the volume of infarct core in dMCAO mice. This investigation provides an appropriate approach for modifying NSCs by LbL assembly using gelatin loaded with VEGF and HA to expedite the rehabilitative ability of engrafted NSCs following ischemic stroke. Graphical abstract Graphical illustration of the fabrication of layer-by-layer (LbL) assembled NSCs tethered with VEGF reservoir [LbL (VEGF)-NSCs], and therapeutic effects of LbL (VEGF)-NSCs on neurovascular network rehabilitation after transplantation in mice with ischemic stroke. Download : Download high-res image (221KB) Download : Download full-size image

quote

GB/T 7714-2015 [1] Hongfei Ge, Quan Hu, Tunan Chen, et al. Applied Materials Today, 2022(28). DOI:10.1016/j.apmt.2022.101548.
MLA [1] Hongfei Ge, et al., Applied Materials Today, no. 28, 2022, https://doi.org/10.1016/j.apmt.2022.101548.
APA [1] Hongfei Ge, Quan Hu, Tunan Chen, Yang Yang, Chao Zhang, Jun Zhong, Yi Yin, Xuheng Jiang, Xin Zhou, Shuhong Wang, Rong Hu, Wenyan Li, & Hua Feng. (2022). Applied Materials Today(28). https://doi.org/10.1016/j.apmt.2022.101548
IEEE [1] Hongfei Ge, Quan Hu, Tunan Chen, Yang Yang, Chao Zhang, Jun Zhong, Yi Yin, Xuheng Jiang, Xin Zhou, Shuhong Wang, Rong Hu, Wenyan Li, and Hua Feng, Applied Materials Today, no. 28, 2022, doi: 10.1016/j.apmt.2022.101548.