Literature DB >> 20533306

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

Xiaogu Wang1, Tetsuo Suzawa, Hirotada Ohtsuka, Baohong Zhao, Yoichi Miyamoto, Tomohiko Miyauchi, Riko Nishimura, Tomio Inoue, Masanori Nakamura, Kazuyoshi Baba, Ryutaro Kamijo.   

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.
© 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20533306     DOI: 10.1002/jcp.22267

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  5 in total

1.  Identification of a pH-responsive DNA region upstream of the transcription start site of human NBCe1-B.

Authors:  Christian M Snead; Susan M Smith; Negar Sadeghein; Rodrigo S Lacruz; Ping Hu; Ira Kurtz; Michael L Paine
Journal:  Eur J Oral Sci       Date:  2011-12       Impact factor: 2.612

2.  Deletion of Slc26a1 and Slc26a7 Delays Enamel Mineralization in Mice.

Authors:  Kaifeng Yin; Jing Guo; Wenting Lin; Sarah Y T Robertson; Manoocher Soleimani; Michael L Paine
Journal:  Front Physiol       Date:  2017-05-16       Impact factor: 4.566

3.  Downregulation of carbonic anhydrase IX promotes Col10a1 expression in chondrocytes.

Authors:  Toshifumi Maruyama; Yoichi Miyamoto; Gou Yamamoto; Atsushi Yamada; Kentaro Yoshimura; Tetsuo Suzawa; Masamichi Takami; Tomohito Akiyama; Marie Hoshino; Fuminori Iwasa; Noriharu Ikumi; Tetsuhiko Tachikawa; Kenji Mishima; Kazuyoshi Baba; Ryutaro Kamijo
Journal:  PLoS One       Date:  2013-02-18       Impact factor: 3.240

4.  SLC26A Gene Family Participate in pH Regulation during Enamel Maturation.

Authors:  Kaifeng Yin; Yuejuan Lei; Xin Wen; Rodrigo S Lacruz; Manoocher Soleimani; Ira Kurtz; Malcolm L Snead; Shane N White; Michael L Paine
Journal:  PLoS One       Date:  2015-12-15       Impact factor: 3.240

5.  MiR-153 Regulates Amelogenesis by Targeting Endocytotic and Endosomal/lysosomal Pathways-Novel Insight into the Origins of Enamel Pathologies.

Authors:  Kaifeng Yin; Wenting Lin; Jing Guo; Toshihiro Sugiyama; Malcolm L Snead; Joseph G Hacia; Michael L Paine
Journal:  Sci Rep       Date:  2017-03-13       Impact factor: 4.379

  5 in total

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