Macrophage Biology Group, Institute for Research in Biomedicine Barcelona, Barcelona, Spain.
Eur J Immunol. 2012 Aug;42(8):1938-48. doi: 10.1002/eji.201242441.
Macrophages play a central role in the immune response. These cells either proliferate in response to, for example, growth factors or become activated in response to, for example, LPS and develop functional activities. Experiments carried out in mice showed that macrophage proliferation requires a short period of ERK phosphorylation, while an extended period is required for macrophage activation. The length of phosphorylation is controlled by the MAPK phosphatase-1 (MKP-1), a nuclear-localized dual-specificity phosphatase that dephosphorylates the MAPKs ERK, p38, and c-Jun NH(2) -terminal kinase (JNK). MKP-1 is induced in macrophages by growth factors, as well as by activators such as LPS, but with different kinetics; to achieve the different functional outcomes (proliferation versus activation), the inhibition of MKP-1 by cytokines such as IFN-γ blocks macrophage proliferation and induces activation. The data presented in this review show that this phosphatase is the switch between macrophage proliferation and activation.
巨噬细胞在免疫反应中起着核心作用。这些细胞要么在生长因子的刺激下增殖,要么在 LPS 等刺激下被激活,从而发展出功能性活动。在小鼠身上进行的实验表明,巨噬细胞的增殖需要 ERK 磷酸化的短时间,而巨噬细胞的激活则需要较长的时间。磷酸化的长度由 MAPK 磷酸酶-1(MKP-1)控制,MKP-1 是一种核定位的双特异性磷酸酶,可使 MAPKs ERK、p38 和 c-Jun NH2 末端激酶(JNK)去磷酸化。MKP-1 可被生长因子以及 LPS 等激活剂诱导,但动力学不同;为了实现不同的功能结果(增殖与激活),细胞因子如 IFN-γ 抑制 MKP-1 可阻断巨噬细胞增殖并诱导其激活。本综述中的数据表明,这种磷酸酶是巨噬细胞增殖和激活之间的开关。