TY - JOUR
T1 - Chronological changes in prosaposin in the developing rat brain
AU - Xue, Bing
AU - Chen, Jie
AU - Gao, Huiling
AU - Saito, Shouichiro
AU - Kobayashi, Naoto
AU - Shimokawa, Tetsuya
AU - Nabeka, Hiroaki
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 to S.M. (No.22591637, 19659380) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
PY - 2011/9
Y1 - 2011/9
N2 - Prosaposin is the precursor protein of four glycoproteins, saposins A, B, C, and D, which activate sphingolipid hydrolases in lysosomes. Besides this role, intact prosaposin is also known as a potent neurotrophic factor that prevents neuronal cell death and stimulates neurite outgrowth in in vivo and in vitro experiments. In the present study, we examined chronological changes in prosaposin immunoreactivity in the rat brain using immunofluorescence staining and Diaminobenzidine (DAB) immunohistochemistry. In the hippocampal regions CA1, CA3, and dentate gyrus, the strongest staining of prosaposin was observed on postnatal day 1. The prosaposin immunoreactivity then decreased gradually until postnatal day 28. But in the cerebral cortex, prosaposin staining intensity increased from postnatal day 1 to 14, then decreased until postnatal day 28. The prosaposin immunoreactivity co-localized with the lysosomal granules labeled by an anti-Cathepsin D antibody, indicating that prosaposin mainly localized in the lysosomes of the neurons. We also examined the chronological changes in prosaposin mRNA and its two alternatively spliced variants using in situ hybridization. We found that both the mRNA forms, especially the one without a nine-base insertion, increased significantly from embryonic day 15 to postnatal day 7, then decreased gradually until postnatal day 28. Abundant prosaposin expression in the perinatal stages indicates a potential role of prosaposin in the early development of the rat brain.
AB - Prosaposin is the precursor protein of four glycoproteins, saposins A, B, C, and D, which activate sphingolipid hydrolases in lysosomes. Besides this role, intact prosaposin is also known as a potent neurotrophic factor that prevents neuronal cell death and stimulates neurite outgrowth in in vivo and in vitro experiments. In the present study, we examined chronological changes in prosaposin immunoreactivity in the rat brain using immunofluorescence staining and Diaminobenzidine (DAB) immunohistochemistry. In the hippocampal regions CA1, CA3, and dentate gyrus, the strongest staining of prosaposin was observed on postnatal day 1. The prosaposin immunoreactivity then decreased gradually until postnatal day 28. But in the cerebral cortex, prosaposin staining intensity increased from postnatal day 1 to 14, then decreased until postnatal day 28. The prosaposin immunoreactivity co-localized with the lysosomal granules labeled by an anti-Cathepsin D antibody, indicating that prosaposin mainly localized in the lysosomes of the neurons. We also examined the chronological changes in prosaposin mRNA and its two alternatively spliced variants using in situ hybridization. We found that both the mRNA forms, especially the one without a nine-base insertion, increased significantly from embryonic day 15 to postnatal day 7, then decreased gradually until postnatal day 28. Abundant prosaposin expression in the perinatal stages indicates a potential role of prosaposin in the early development of the rat brain.
KW - Alternative splicing
KW - Autocrine
KW - Hippocampus
KW - Immunofluorescence staining
KW - Immunohistochemistry
KW - In situ hybridization
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U2 - 10.1016/j.neures.2011.06.001
DO - 10.1016/j.neures.2011.06.001
M3 - Article
C2 - 21684311
AN - SCOPUS:79960896237
SN - 0168-0102
VL - 71
SP - 22
EP - 34
JO - Neuroscience Research
JF - Neuroscience Research
IS - 1
ER -