Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10770623 | Biochemical and Biophysical Research Communications | 2005 | 7 Pages |
Abstract
The addition of lecithin molecules to brain-derived neurotrophic factor (BDNF) has been reported to markedly enhance its pharmacological effect in vivo. In the current study, we show that lecithinized BDNF (PC-BDNF) has a higher affinity than BDNF for neural precursor cells. Although BDNF only slightly increased the expression of the genes for Mash-1, p35, 68Â kDa neurofilament, and TrkB receptor, PC-BDNF caused a significant increase in their expression. PC-BDNF also increased the level of neurofilament protein and dramatically increased TrkB mRNA gene expression, which was followed by a sustained activation of the p42/p44 extracellular-regulated kinases. Finally, transplantation of PC-BDNF-treated cells was more effective than BDNF-treated cells at improving impaired motor function caused by spinal cord injury. These findings showed that PC-BDNF has a better potential than BDNF for promoting neural differentiation, partly due to a higher cellular affinity. Furthermore, PC-BDNF-treated cells could be useful for transplantation therapy for central nervous system injuries.
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Authors
Aki Kitagawa, Toshiaki Nakayama, Mitsuko Takenaga, Kayo Matsumoto, Yukie Tokura, Yuki Ohta, Manabu Ichinohe, Yoko Yamaguchi, Noboru Suzuki, Hideyuki Okano, Rie Igarashi,