VanUffelen B E, de Koster B M, VanSteveninck J, Elferink J G
Department of Medical Biochemistry, Leiden University, The Netherlands.
Inflamm Res. 1997 Oct;46(10):427-9. doi: 10.1007/s000110050218.
To study the effect of cyclic nucleotides and PDE-resistant cyclic nucleotide analogues on neutrophil migration.
Migration of electropermeabilized neutrophils in Boyden chambers in vitro.
Addition of cyclic AMP inhibited migration of electropermeabilized neutrophils in the presence of cGMP, relative to the level of migration in the presence of cGMP alone. However, when cGMP was replaced with 8-pCPT-cGMP or Sp-cGMPS, analogues of cGMP which are not degraded by phosphodiesterases, cAMP synergistically enhanced migration. In contrast, migration in the presence of the phosphodiesterase-resistant cAMP analogue, Sp-cAMPS, was not enhanced by addition of cGMP.
Taking into account reports in the literature which show that cGMP-hydrolysing activity can be enhanced by the catalytic subunit of cAMP-dependent protein kinase, it is hypothesized that breakdown of cGMP in neutrophils may be modulated via cAMP.
研究环核苷酸及磷酸二酯酶抗性环核苷酸类似物对中性粒细胞迁移的影响。
体外电穿孔中性粒细胞在博伊登小室中的迁移。
相对于仅存在环鸟苷酸(cGMP)时的迁移水平,在存在cGMP的情况下添加环腺苷酸(cAMP)可抑制电穿孔中性粒细胞的迁移。然而,当用8 - 对氯苯硫基 - cGMP或Sp - cGMPS(cGMP的类似物,不被磷酸二酯酶降解)替代cGMP时,cAMP可协同增强迁移。相反,添加cGMP不会增强磷酸二酯酶抗性cAMP类似物Sp - cAMPS存在时的迁移。
考虑到文献报道显示cAMP依赖性蛋白激酶的催化亚基可增强cGMP水解活性,推测中性粒细胞中cGMP的分解可能通过cAMP进行调节。