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Gelatin Nanostructured Lipid Carriers Incorporating Nerve Growth Factor Inhibit Endoplasmic Reticulum Stress-Induced Apoptosis and Improve Recovery in Spinal Cord Injury.

Authors :
Zhu, Si-Pin
Wang, Zhou-Guang
Zhao, Ying-Zheng
Wu, Jiang
Shi, Hong-Xue
Ye, Li-Bing
Wu, Fen-Zan
Cheng, Yi
Zhang, Hong-Yu
He, Songbin
Wei, Xiaojie
Fu, Xiao-Bing
Li, Xiao-Kun
Xu, Hua-Zi
Xiao, Jian
Source :
Molecular Neurobiology; Sep2016, Vol. 53 Issue 7, p4375-4386, 12p
Publication Year :
2016

Abstract

Clinical translation of growth factor therapies faces multiple challenges; the most significant one is the short half-life of the naked protein. Gelatin nanostructured lipid carriers (GNLs) had previously been used to encapsulate the basic fibroblast growth factor to enhance the functional recovery in hemiparkinsonian rats. In this research, we comparatively study the enhanced therapy between nerve growth factor (NGF) loaded GNLs (NGF-GNLs) and NGF only in spinal cord injury (SCI). The effects of NGF-GNLs and NGF only were tested by the Basso-Beattie-Bresnahan (BBB) locomotion scale, inclined plane test, and footprint analysis. Western blot analysis and immunofluorescent staining were further performed to identify the expression of ER stress-related proteins, neuron-specific marker neuronal nuclei (NeuN), and growth-associated protein 43 (GAP43). Correlated downstream signals Akt/GSK-3β and ERK1/2 were also analyzed with or without inhibitors. Results showed that NGF-GNLs, compared to NGF only, enhanced the neuroprotection effect in SCI rats. The ER stress-induced apoptosis response proteins CHOP, GRP78 and caspase-12 inhibited by NGF-GNL treatment were more obvious. Meanwhile, NGF-GNLs in the recovery of SCI are related to the inhibition of ER stress-induced cell death via the activation of downstream signals PI3K/Akt/GSK-3β and ERK1/2. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08937648
Volume :
53
Issue :
7
Database :
Complementary Index
Journal :
Molecular Neurobiology
Publication Type :
Academic Journal
Accession number :
117065869
Full Text :
https://doi.org/10.1007/s12035-015-9372-2