[Effect of Naoluo Xintong on proliferation and differentiation of neural stem cells and β-tubulin Ⅲ/GFAP].

OBJECTIVE To observe the effects of Naoluo Xintong on the expression of β-tubulin Ⅲ and glial fibrillary acidic protein (GFAP) and the proliferation and differentiation of murine neural stem cells (NSCs) in vitro. METHODS An immortalized murine NSC line was divided into model control (MC) group, 10% Naoluo Xintong drug-containing serum group (NLXT group), and 10% Naoluoxintong drug-containing serum with inhibitor Y27632 group (Y-27632 group) with corresponding treatments. The activity of the NSCs was detected after the treatments using MTT assay, and the migration of the cells was observed with Transwell assay. The expressions of β-tubulin Ⅲ, GFAP and MAP-2 proteins in the cells were detected with immunoblotting, and the expressions of DCX, NEUN, and β-tubulin Ⅲ were also detected with immunofluorescence assay. RESULTS Compared with that in MC group, the number of migrated cells in NLXT group and Y-27632 group increased significantly at 1 day and 3 days after induction (P < 0.05). The survival rate and the number of migrated cells in NLXT group and Y-27632 group increased significantly on day 7 (P < 0.01). Compared with those in MC group, the expressions of β-tubulin Ⅲ, MAP2 and GFAP protein in NLXT group and Y-27632 group were significantly increased on days 3 (P < 0.01) and 7 (P < 0.05). The numbers of β-tubulinⅢ/ GFAP, BrdU/DCX, and BrdU/NEUN labeled cells in the NLXT group and Y-27632 group were significantly greater than those in the MC group. CONCLUSIONS Naoluo Xintong promotes the proliferation and differentiation of murine NSCs in vitro by regulating the expressions of β-tubulinⅢ/GFAP.

[1]  Shuxiong Zeng,et al.  Protective effects of primary neural stem cell treatment in ischemic stroke models , 2018, Experimental and therapeutic medicine.

[2]  Wengui Yu,et al.  Stenting for intracranial stenosis: potential future for the prevention of disabling or fatal stroke , 2018, Stroke and Vascular Neurology.

[3]  Adrián García-Concejo,et al.  Morphine delays neural stem cells differentiation by facilitating Nestin overexpression. , 2018, Biochimica et biophysica acta. General subjects.

[4]  W. Xia,et al.  Adjudin-preconditioned neural stem cells enhance neuroprotection after ischemia reperfusion in mice , 2017, Stem Cell Research & Therapy.

[5]  Wei Zhang,et al.  Nestin regulates neural stem cell migration via controlling the cell contractility. , 2016, The international journal of biochemistry & cell biology.

[6]  R. Rola,et al.  ACEA (a highly selective cannabinoid CB1 receptor agonist) stimulates hippocampal neurogenesis in mice treated with antiepileptic drugs , 2015, Brain Research.

[7]  T. Saido,et al.  Involvement of calpains in adult neurogenesis: implications for stroke , 2015, Front. Cell. Neurosci..

[8]  W. Young,et al.  Coexpression of Angiopoietin-1 with VEGF Increases the Structural Integrity of the Blood–Brain Barrier and Reduces Atrophy Volume , 2011, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[9]  R. McKay,et al.  Efficient generation of midbrain and hindbrain neurons from mouse embryonic stem cells , 2000, Nature Biotechnology.

[10]  Alican Tahta,et al.  Assessment of the MRI and Behavioral Test Results in a Focal Cerebral Ischemia-Reperfusion Model in the Rat after Separate and Combined Use of Mouse-Derived Neural Progenitor Cells, Human-Derived Neural Progenitor Cells and Atorvastatin. , 2017, Turkish Neurosurgery.