Effect of low-intensity pulsed ultrasound on the expression of neurotrophin-3 and brain-derived neurotrophic factor in cultured Schwann cells

✍ Scribed by Hua Zhang; Xin Lin; Hong Wan; Jun-Hua Li; Jia-Mou Li

• Publisher: John Wiley and Sons
• Year: 2009
• Tongue: English
• Weight: 179 KB
• Volume: 29
• Category: Article
• ISSN: 0738-1085
• DOI: 10.1002/micr.20644

✦ Synopsis

Abstract

It is generally known that low‐intensity pulsed ultrasound (LIPUS) accelerates peripheral nerve tissue regeneration. However, the precise cellular mechanism involved is still unclear. The purpose of this study was to determine how the Schwann cells respond directly to LIPUS stimuli. Thus, we investigated the effect of LIPUS on cell proliferation, neurotrophin‐3 (NT‐3), and brain‐derived neurotrophic factor (BDNF) mRNA expression in rat Schwann cells. Schwann cells were enzymatically isolated from postnatal 1–3 day rat sciatic nerve tissue and cultured in the six‐well plate. The ultrasound was applied at a frequency of 1 MHz and an intensity of 100 mW/cm^2^ spatial average temporal average for 5 minutes/day. The control group was cultured in the same way but without the administration of ultrasound. Immunohistochemistry demonstrated that more than 98% of the experimental and control cells were positive for S‐100, NT‐3, and BDNF. With 5‐bromo‐2′‐deoxyuridine (BrdU) assay, the stimulated cells also exhibited an increase in the rate of cell proliferation on days 4, 7, 10, and 14. Further investigation found that mRNA expression of NT‐3 was significantly upregulated in experimental groups compared with the control 14 days after the LIPUS stimulation (the ratio of NT‐3/β‐actin was 0.56 ± 0.13 vs. 0.41 ± 0.09, P < 0.01), whereas the mRNA expression of BDNF was significantly downregulated in experimental groups compared with the control (the ratio of BDNF/β‐actin was 0.51 ± 0.05 vs. 0.60 ± 0.08, P < 0.05). These results demonstrated that the application of LIPUS promotes cell proliferation and NT‐3 gene expression in Schwann cells, and involved in the alteration of BDNF gene expression. © 2009 Wiley‐Liss, Inc. Microsurgery, 2009.