Nishio H, Matsui K, Tsuji H, Tamura A, Suzuki K
Department of Legal Medicine, Osaka Medical College, Takatsuki, Japan.
Acta Histochem. 2001 Feb;103(1):89-98. doi: 10.1078/0065-1281-00581.
In the present study, we investigated the immunohistochemical localization of mitogen-activated protein kinase (MAPK) signaling pathway in the human thymus. Three members of MAPK, the extracellular signal-regulated kinase (ERK), the c-Jun N-terminal kinase (JNK) and the p38 kinase, showed differential expression patterns in the thymus medulla. The phosphorylated form of ERK (p-ERK) was abundantly present in the outer layer of Hassall's corpuscles, and the phosphorylated form of p38 kinase (p-p38 kinase) was present in the entire Hassall's corpuscles. The phosphorylated form of JNK (p-JNK) was expressed in medullary thymocytes. We also examined localization of MAPK kinases (MAPKK or MEK) which specifically activate MAPK. MEK1, an activator of ERK, was found in the outer layer of Hassall's corpuscles where p-ERK was expressed. MEK3, an activator of p38 kinase, was also expressed in the outer layer. MEK4 and MEK7, which are activators of JNK, were present in the entire Hassall's corpuscles. Thus, differential expression of MAPK in the thymus supports the concept that the MAPK signaling pathway controls the specificity of functional thymic responses to extracellular stimuli. Furthermore, the abundant expression of various elements of the pathway in Hassall's corpuscles suggests that the pathway is involved in thymic medullary epithelial maturation.
在本研究中,我们调查了丝裂原活化蛋白激酶(MAPK)信号通路在人胸腺中的免疫组织化学定位。MAPK的三个成员,即细胞外信号调节激酶(ERK)、c-Jun氨基末端激酶(JNK)和p38激酶,在胸腺髓质中呈现出不同的表达模式。ERK的磷酸化形式(p-ERK)大量存在于哈氏小体的外层,p38激酶的磷酸化形式(p-p38激酶)存在于整个哈氏小体中。JNK的磷酸化形式(p-JNK)在髓质胸腺细胞中表达。我们还检测了特异性激活MAPK的MAPK激酶(MAPKK或MEK)的定位。ERK的激活剂MEK1在表达p-ERK的哈氏小体外层被发现。p38激酶的激活剂MEK3也在外层表达。JNK的激活剂MEK4和MEK7存在于整个哈氏小体中。因此,MAPK在胸腺中的差异表达支持了MAPK信号通路控制胸腺对细胞外刺激的功能性反应特异性这一概念。此外,该信号通路的各种元件在哈氏小体中的大量表达表明该信号通路参与胸腺髓质上皮细胞的成熟。