Clinical application of seminal plasma sperm motility inhibitor.
| Project/Area Number |
06454461
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Urology
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| Research Institution | St.Marianna University School of Medicine |
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Principal Investigator |
IWAMOTO Teruaki St.Marianna Univ., Urology, Professor., 医学部, 教授 (60046117)
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| Co-Investigator(Kenkyū-buntansha) |
FURUICHI Yasuhiro AGENE Research institute, Director, 所長
TANAKA Hiroki St.Marianna Univ., Urology, Instructor, 医学部, 助手 (00217069)
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| Project Period (FY) |
1994 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥7,200,000 (Direct Cost: ¥7,200,000)
Fiscal Year 1996: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 1995: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1994: ¥4,300,000 (Direct Cost: ¥4,300,000)
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| Keywords | Seminal plasma sperm motility inhibitor / Seminal vesicle / Seminal plasma / Asthenozoospermia / Dynein arm / Semenogelin / basic protein / Sperm adhesin family / cDNA / 除膜精子 |
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| Research Abstract |
1. We described the primary structure of SPMI,the coding of boar SPMI cDNA gene, Nucleotide sequence analysis of the 645-bp SPMI cDNA predicts a coded polypeptide of 137 amino acid residues which includes a 21-residue signal peptide and a 116 residues secreted protein. The amino acid sequence of SPMI was found to be highly homologous to AQN-3, a member of spermadhesin family proteins of boar that bind to spermatozoa. Expression of the boar SPMI gene detected by Northern blot analysis revealed that its expression is very abundunt in seminal vesicles and specific to this tissue.
2. When SPMI was reacted with normal motile sperm, the motility was inhibited in a dose-dependent manner, and completely suppressed at a SPMI concentration of 1500U/ml. After immediate washing of the immotilized sperm, they resumed movement and recovered 30% motility. However, motility was not recovered at a SPMI concentration of 2000U/ml or more. The mechanism of the inhibition of sperm motility was immunohistochemically examined at electron microscopic level using anti-boar SPMI antibody. SPMI was stained on the surface cell membrane of sperm and not stained on inside cell. SPMI did not penetrate the sperm cell membrane. These findings suggest that sperm can not move physically by the attachment of SPMI to cell membrane or second messenger from the sperm cell membrane attached with SPMI inhibits the activity of dynein ATPase.
3. Human SPMI precursor identifies with Semenogelin I,II.We investigated whether gene structure of Semenogelin I,II on infertile patients is different with that on fertile men. Two infertile patients and one fertile man had a deletion of same size, 180bp of Semenogelin I DNA.This deletion of gene was not specific in infetile patients.
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Report
(4 results)
Research Products
(11 results)
