TY - JOUR
T1 - Expression patterns in alternative splicing forms of prosaposin mRNA in the rat facial nerve nucleus after facial nerve transection
AU - Chen, Jie
AU - Saito, Shouichiro
AU - Kobayashi, Naoto
AU - Sato, Kohji
AU - Terashita, Takehiro
AU - Shimokawa, Tetsuya
AU - Mominoki, Katsumi
AU - Miyawaki, Kyojy
AU - Sano, Akira
AU - Matsuda, Seiji
N1 - Funding Information:
We thank S. Masuda (INCS, Ehime University) and C. Kanaka (Department of Anatomy and Neuroscience, Hamamatsu University School of Medicine) for their technical assistance. This study was supported in part by Grants-in-Aid for Scientific Research (B) to SM from the Japan Society for the Promotion of Science. J. Chen received a Japanese government grant awarded to foreign students.
PY - 2008/1
Y1 - 2008/1
N2 - Prosaposin acts as a neurotrophic factor, in addition to its role as the precursor protein for saposins A, B, C, and D, which are activators for specific sphingolipid hydrolases in lysosomes. In rats, the prosaposin gene generates two alternative splicing forms of mRNA: Pro + 9 containing a 9-base insertion and Pro + 0 without. The expression of these mRNAs changes after brain injury. We examined the expression patterns of the alternative splicing forms of prosaposin mRNA in the rat facial nerve nucleus for 52 days following facial nerve transection. Pro + 0 mRNA increased within 3 days of transection, peaked after 5-10 days, and remained significantly elevated for 21 days. In contrast, the expression of Pro + 9 mRNA was constant throughout the regenerative period. Prosaposin mRNA expression increased not only in facial motoneurons, but also in microglia during facial nerve regeneration. Our findings indicate that the saposin B domain of prosaposin, which is the domain affected by alternative splicing, plays an important role in both neurons and microglia during neuroregeneration.
AB - Prosaposin acts as a neurotrophic factor, in addition to its role as the precursor protein for saposins A, B, C, and D, which are activators for specific sphingolipid hydrolases in lysosomes. In rats, the prosaposin gene generates two alternative splicing forms of mRNA: Pro + 9 containing a 9-base insertion and Pro + 0 without. The expression of these mRNAs changes after brain injury. We examined the expression patterns of the alternative splicing forms of prosaposin mRNA in the rat facial nerve nucleus for 52 days following facial nerve transection. Pro + 0 mRNA increased within 3 days of transection, peaked after 5-10 days, and remained significantly elevated for 21 days. In contrast, the expression of Pro + 9 mRNA was constant throughout the regenerative period. Prosaposin mRNA expression increased not only in facial motoneurons, but also in microglia during facial nerve regeneration. Our findings indicate that the saposin B domain of prosaposin, which is the domain affected by alternative splicing, plays an important role in both neurons and microglia during neuroregeneration.
KW - Facial nerve nucleus
KW - In situ hybridization
KW - Microglia
KW - Neuroregeneration
KW - Neurotrophic factor
KW - Saposin B
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U2 - 10.1016/j.neures.2007.09.010
DO - 10.1016/j.neures.2007.09.010
M3 - Article
C2 - 18022721
AN - SCOPUS:37549026431
SN - 0168-0102
VL - 60
SP - 82
EP - 94
JO - Neuroscience Research
JF - Neuroscience Research
IS - 1
ER -