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碳酸酐酶 II 通过细胞内 pH 依赖的 JNK 信号通路调节成釉细胞的分化。

Carbonic anhydrase II regulates differentiation of ameloblasts via intracellular pH-dependent JNK signaling pathway.

机构信息

Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan.

出版信息

J Cell Physiol. 2010 Nov;225(3):709-19. doi: 10.1002/jcp.22267.

Abstract

Differentiation of ameloblasts from undifferentiated epithelial cells is controlled by diverse growth factors, as well as interactions between epithelium and mesenchyme. However, there is a considerable lack of knowledge regarding the precise mechanisms that control ameloblast differentiation and enamel biomineralization. We found that the expression level of carbonic anhydrase II (CAII) is strongly up-regulated in parallel with differentiation of enamel epithelium tissues, while the enzyme activity of CA was also increased along with differentiation in ameloblast primary cultures. The expression level of amelogenin, a marker of secretory-stage ameloblasts, was enhanced by ethoxzolamide (EZA), a CA inhibitor, as well as CAII antisense (CAIIAS), whereas the expression of enamel matrix serine proteinase-1 (EMSP-1), a marker for maturation-stage ameloblasts, was suppressed by both. These agents also promoted ameloblast proliferation. In addition, inhibition of ameloblast differentiation by EZA and CAIIAS was confirmed using tooth germ organ cultures. Furthermore, EZA and CAIIAS elevated intracellular pH in ameloblasts, while experimental decreases in intracellular pH abolished the effect of CAIIAS on ameloblasts and triggered the activation of c-Jun N-terminal kinase (JNK). SP600125, a JNK inhibitor, abrogated the response of ameloblasts to an experimental decrease in intracellular pH, while the inhibition of JNK also impaired ameloblast differentiation. These results suggest a novel role for CAII during amelogenesis, that is, controlling the differentiation of ameloblasts. Regulation of intracellular pH, followed by activation of the JNK signaling pathway, may be responsible for the effects of CAII on ameloblasts.

摘要

成釉细胞从未分化的上皮细胞分化是由多种生长因子控制的,以及上皮和间充质之间的相互作用。然而,对于控制成釉细胞分化和釉质生物矿化的确切机制,我们知之甚少。我们发现碳酸酐酶 II(CAII)的表达水平与釉质上皮组织的分化呈强烈的平行上调,而在成釉细胞原代培养中,随着分化的进行,CA 的酶活性也增加了。釉原蛋白是分泌期成釉细胞的标志物,其表达水平被 CA 抑制剂乙氧唑胺(EZA)和 CAII 反义(CAIIAS)增强,而成熟期成釉细胞的标志物釉基质丝氨酸蛋白酶-1(EMSP-1)的表达则受到两者的抑制。这些试剂也促进了成釉细胞的增殖。此外,在牙胚器官培养中证实了 EZA 和 CAIIAS 对成釉细胞分化的抑制作用。此外,EZA 和 CAIIAS 提高了成釉细胞内的 pH 值,而实验性降低细胞内 pH 值则消除了 CAIIAS 对成釉细胞的作用,并触发了 c-Jun N-末端激酶(JNK)的激活。JNK 抑制剂 SP600125 消除了成釉细胞对细胞内 pH 值降低的反应,而 JNK 的抑制也损害了成釉细胞的分化。这些结果表明 CAII 在釉质发生过程中具有新的作用,即控制成釉细胞的分化。细胞内 pH 值的调节,随后是 JNK 信号通路的激活,可能是 CAII 对成釉细胞作用的原因。

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