Neural Growth Factor Stimulates Proliferation of Spinal Cord Derived-Neural Precursor/Stem Cells.
10.3340/jkns.2016.59.5.437
- Author:
Youngmin HAN
1
;
Kyoung Tae KIM
Author Information
1. Department of Neurosurgery, Kyungpook National University Hospital, Daegu, Korea. nskimkt7@gmail.com
- Publication Type:Original Article
- Keywords:
Neural growth factor;
Spinal cord neural precursor/stem cell;
Spinal cord injury
- MeSH:
Animals;
Brain;
Cartilage;
Cell Proliferation;
Central Nervous System;
Gene Expression;
Humans;
Immunohistochemistry;
In Vitro Techniques;
Microscopy;
Nerve Growth Factor;
Nestin;
Rats;
Spinal Cord Injuries;
Spinal Cord*
- From:Journal of Korean Neurosurgical Society
2016;59(5):437-441
- CountryRepublic of Korea
- Language:English
-
Abstract:
OBJECTIVE: Recently, regenerative therapies have been used in clinical trials (heart, cartilage, skeletal). We don't make use of these treatments to spinal cord injury (SCI) patients yet, but regenerative therapies are rising interest in recent study about SCI. Neural precursor/stem cell (NPSC) proliferation is a significant event in functional recovery of the central nervous system (CNS). However, brain NPSCs and spinal cord NPSCs (SC-NPSCs) have many differences including gene expression and proliferation. The purpose of this study was to investigate the influence of neural growth factor (NGF) on the proliferation of SC-NPSCs. METHODS: NPSCs (2×10⁴) were suspended in 100 µL of neurobasal medium containing NGF-7S (Sigma-Aldrich) and cultured in a 96-well plate for 12 days. NPSC proliferation was analyzed five times for either concentration of NGF (0.02 and 2 ng/mL). Sixteen rats after SCI were randomly allocated into two groups. In group 1 (SCI-vehicle group, n=8), animals received 1.0 mL of the saline vehicle solution. In group 2 (SCI-NGF group, n=8), the animals received single doses of NGF (Sigma-Aldrich). A dose of 0.02 ng/mL of NGF or normal saline as a vehicle control was intra-thecally injected daily at 24 hour intervals for 7 days. For Immunohistochemistry analysis, rats were sacrificed after one week and the spinal cords were obtained. RESULTS: The elevation of cell proliferation with 0.02 ng/mL NGF was significant (p<0.05) but was not significant for 2 ng/mL NGF. The optical density was increased in the NGF 0.02 ng/mL group compared to the control group and NGF 2 ng/mL groups. The density of nestin in the SCI-NGF group was significantly increased over the SCI-vehicle group (p<0.05). High power microscopy revealed that the density of nestin in the SCI-NGF group was significantly increased over the SCI-vehicle group. CONCLUSION: SC-NPSC proliferation is an important pathway in the functional recovery of SCI. NGF enhances SC-NPSC proliferation in vitro and in vivo. NGF may be a useful option for treatment of SCI patients pending further studies to verify the clinical applicability.
