Dusi S, Donini M, Rossi F
Institute of General Pathology, University of Verona, Italy.
Biochem J. 1994 Nov 15;304 ( Pt 1)(Pt 1):243-50. doi: 10.1042/bj3040243.
Challenge of neutrophils with concanavalin A (ConA), formyl-methionyl-leucyl-phenylalanine (FMLP), and phorbol 12-myristate 13-acetate (PMA) induced the tyrosine phosphorylation of several proteins. Among these proteins we have identified two mitogen-activated protein kinase (MAPK) isoforms of 43 kDa (p43 MAPK) and 45 kDa (p45 MAPK) molecular mass. Moreover here we show that: (1) FMLP induced the tyrosine phosphorylation of the p43 MAPK, and ConA that of p45 MAPK, while PMA induced the tyrosine phosphorylation of both p43 and p45 MAPK; all these agonists induced the tyrosine phosphorylation of a 75 kDa protein (p75). (2) With FMLP or ConA as agonists, tyrosine phosphorylations of MAPK and p75 can be involved in the process of NADPH oxidase activation. On the contrary, PMA can activate the respiratory burst independently of these phosphorylations. (3) In Ca(2+)-depleted neutrophils, where phospholipid hydrolysis did not take place, ConA or FMLP did not activate the respiratory burst, but while ConA induced the tyrosine phosphorylation of p45 MAPK and p75, FMLP was not able to phosphorylate p43 MAPK and p75. (4) As previously observed in our laboratory, a double stimulation of Ca(2+)-depleted neutrophils with ConA plus FMLP induced a respiratory burst in the absence of activation of second messengers derived from phospholipase C, D and A2 activity. This respiratory burst was accompanied by tyrosine phosphorylation of both p43 and p45 MAPKs. These results indicate that when FMLP is the agonist, both the tyrosine phosphorylation of p43 MAPK and p75, and the activation of NADPH oxidase, are coupled to Ca(2+)-dependent mechanisms. On the contrary, ConA can induce the tyrosine phosphorylation of p45 MAPK and p75 independently of calcium, but an unknown Ca(2+)-dependent mechanism is necessary for the activation of NADPH oxidase by this agonist. This mechanism could be substituted by the induction of tyrosine phosphorylation of both p43 MAPK and p45 MAPK when Ca(2+)-depleted neutrophils are stimulated with ConA plus FMLP.
用刀豆球蛋白A(ConA)、甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)和佛波酯(PMA)刺激中性粒细胞,可诱导多种蛋白质的酪氨酸磷酸化。在这些蛋白质中,我们鉴定出了两种分子量分别为43 kDa(p43 MAPK)和45 kDa(p45 MAPK)的丝裂原活化蛋白激酶(MAPK)亚型。此外,我们在此表明:(1)FMLP诱导p43 MAPK的酪氨酸磷酸化,ConA诱导p45 MAPK的酪氨酸磷酸化,而PMA诱导p43和p45 MAPK的酪氨酸磷酸化;所有这些激动剂均诱导一种75 kDa蛋白质(p75)的酪氨酸磷酸化。(2)以FMLP或ConA作为激动剂时,MAPK和p75的酪氨酸磷酸化可参与NADPH氧化酶的激活过程。相反,PMA可独立于这些磷酸化作用激活呼吸爆发。(3)在缺乏Ca²⁺的中性粒细胞中,磷脂水解未发生,ConA或FMLP未激活呼吸爆发,但ConA诱导p45 MAPK和p75的酪氨酸磷酸化,而FMLP无法使p43 MAPK和p75磷酸化。(4)如我们实验室之前所观察到的,用ConA加FMLP对缺乏Ca²⁺的中性粒细胞进行双重刺激,在未激活源自磷脂酶C、D和A2活性的第二信使的情况下诱导了呼吸爆发。这种呼吸爆发伴随着p43和p45 MAPKs的酪氨酸磷酸化。这些结果表明,当FMLP作为激动剂时,p43 MAPK和p75的酪氨酸磷酸化以及NADPH氧化酶的激活均与Ca²⁺依赖性机制相关。相反,ConA可独立于钙诱导p45 MAPK和p75的酪氨酸磷酸化,但该激动剂激活NADPH氧化酶需要一种未知的Ca²⁺依赖性机制。当用ConA加FMLP刺激缺乏Ca²⁺的中性粒细胞时,这种机制可被p43 MAPK和p45 MAPK的酪氨酸磷酸化诱导所替代。