Effect of substance P and protein kinase inhibitors on β-amyloid peptide-induced proliferation of cultured brain cells

Vijendra K. Singh, Jui Fen Cheng, Sy Jye C Leu

研究成果: 雜誌貢獻文章

21 引文 (Scopus)

摘要

The present study investigated the effect of substance P (SP) and protein kinase inhibitors (H7 and HA1004) on β-amyloid peptide-induced proliferation of neonatal rat brain cells in primary cultures. The β-amyloid peptide1-28 (designated as βAP28), at nanomolar concentrations (10-9 M), significantly (P {precedes above single-line equals sign} 0.05) increased the proliferation of brain cells (presumably non-neuronal) as measured by [3H]thymidine uptake into DNA (mitogenesis). The effect was dependent on time of cultured, concentration of βAP28, and presence of fetal calf serum. The supplementation of SP into cell cultures at time zero reversed the proliferative response of βAP28. Moreover, the βAP28-induced proliferation was inhibited by protein kinase inhibitor H7, but not by HA1004. Since H7 is a selective protein kinase C (PKC) inhibitor and SP action involves PKC, we conclude that βAP28 induces normal brain cell proliferation through PKC pathway of cell signaling.

原文英語
頁(從 - 到)353-356
頁數4
期刊Brain Research
660
發行號2
DOIs
出版狀態已發佈 - 十月 17 1994
對外發佈Yes

指紋

Protein Kinase Inhibitors
Substance P
Amyloid
Protein Kinase C
Cultured Cells
Peptides
Brain
Cell Proliferation
Primary Cell Culture
Protein C Inhibitor
Thymidine
Cell Culture Techniques
DNA
Serum

ASJC Scopus subject areas

  • Developmental Biology
  • Molecular Biology
  • Clinical Neurology
  • Neuroscience(all)

引用此文

Effect of substance P and protein kinase inhibitors on β-amyloid peptide-induced proliferation of cultured brain cells. / Singh, Vijendra K.; Cheng, Jui Fen; Leu, Sy Jye C.

於: Brain Research, 卷 660, 編號 2, 17.10.1994, p. 353-356.

研究成果: 雜誌貢獻文章

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