Zinc transport complexes contribute to the homeostatic maintenance of secretory pathway function in vertebrate cells - PubMed (original) (raw)
. 2006 Jun 30;281(26):17743-50.
doi: 10.1074/jbc.M602470200. Epub 2006 Apr 24.
Affiliations
- PMID: 16636052
- DOI: 10.1074/jbc.M602470200
Free article
Zinc transport complexes contribute to the homeostatic maintenance of secretory pathway function in vertebrate cells
Kaori Ishihara et al. J Biol Chem. 2006.
Free article
Abstract
Zinc transporters play important roles in a wide range of biochemical processes. Here we report an important function of ZnT5/ZnT6 hetero-oligomeric complexes in the secretory pathway. The activity of human tissue-nonspecific alkaline phosphatase (ALP) expressed in ZnT5(-)ZnT7(-/-) cells was significantly reduced compared with that expressed in wild-type cells as in the case of endogenous chicken tissue-nonspecific ALP activity. The inactive human tissue-nonspecific ALP in ZnT5(-)ZnT7(-/-) cells was degraded by proteasome-mediated degradation without being trafficked to the plasma membrane. ZnT5(-)ZnT7(-/-) cells showed exacerbation of the unfolded protein response as did the wild-type cells cultured under a zinc-deficient condition, revealing that both complexes play a role in homeostatic maintenance of secretory pathway function. Furthermore, we showed that expression of ZnT5 mRNA was up-regulated by the endoplasmic reticulum stress in various cell lines. The up-regulation of the hZnT5 transcript was mediated by transcription factor XBP1 through the TGACGTGG sequence in the hZnT5 promoter, and this sequence was highly conserved in the ZnT5 genes of mouse and chicken. These results suggest that zinc transport into the secretory pathway is strictly regulated for the homeostatic maintenance of secretory pathway function in vertebrate cells.
Similar articles
- Two different zinc transport complexes of cation diffusion facilitator proteins localized in the secretory pathway operate to activate alkaline phosphatases in vertebrate cells.
Suzuki T, Ishihara K, Migaki H, Ishihara K, Nagao M, Yamaguchi-Iwai Y, Kambe T. Suzuki T, et al. J Biol Chem. 2005 Sep 2;280(35):30956-62. doi: 10.1074/jbc.M506902200. Epub 2005 Jul 1. J Biol Chem. 2005. PMID: 15994300 - Zinc transporters, ZnT5 and ZnT7, are required for the activation of alkaline phosphatases, zinc-requiring enzymes that are glycosylphosphatidylinositol-anchored to the cytoplasmic membrane.
Suzuki T, Ishihara K, Migaki H, Matsuura W, Kohda A, Okumura K, Nagao M, Yamaguchi-Iwai Y, Kambe T. Suzuki T, et al. J Biol Chem. 2005 Jan 7;280(1):637-43. doi: 10.1074/jbc.M411247200. Epub 2004 Nov 2. J Biol Chem. 2005. PMID: 15525635 - Detailed analyses of the crucial functions of Zn transporter proteins in alkaline phosphatase activation.
Suzuki E, Ogawa N, Takeda TA, Nishito Y, Tanaka YK, Fujiwara T, Matsunaga M, Ueda S, Kubo N, Tsuji T, Fukunaka A, Yamazaki T, Taylor KM, Ogra Y, Kambe T. Suzuki E, et al. J Biol Chem. 2020 Apr 24;295(17):5669-5684. doi: 10.1074/jbc.RA120.012610. Epub 2020 Mar 16. J Biol Chem. 2020. PMID: 32179649 Free PMC article. - An overview of a wide range of functions of ZnT and Zip zinc transporters in the secretory pathway.
Kambe T. Kambe T. Biosci Biotechnol Biochem. 2011;75(6):1036-43. doi: 10.1271/bbb.110056. Epub 2011 Jun 13. Biosci Biotechnol Biochem. 2011. PMID: 21670538 Review. - Understanding the Contribution of Zinc Transporters in the Function of the Early Secretory Pathway.
Kambe T, Matsunaga M, Takeda TA. Kambe T, et al. Int J Mol Sci. 2017 Oct 19;18(10):2179. doi: 10.3390/ijms18102179. Int J Mol Sci. 2017. PMID: 29048339 Free PMC article. Review.
Cited by
- Direct Comparison of Manganese Detoxification/Efflux Proteins and Molecular Characterization of ZnT10 Protein as a Manganese Transporter.
Nishito Y, Tsuji N, Fujishiro H, Takeda TA, Yamazaki T, Teranishi F, Okazaki F, Matsunaga A, Tuschl K, Rao R, Kono S, Miyajima H, Narita H, Himeno S, Kambe T. Nishito Y, et al. J Biol Chem. 2016 Jul 8;291(28):14773-87. doi: 10.1074/jbc.M116.728014. Epub 2016 May 10. J Biol Chem. 2016. PMID: 27226609 Free PMC article. - The ins and outs of algal metal transport.
Blaby-Haas CE, Merchant SS. Blaby-Haas CE, et al. Biochim Biophys Acta. 2012 Sep;1823(9):1531-52. doi: 10.1016/j.bbamcr.2012.04.010. Epub 2012 May 1. Biochim Biophys Acta. 2012. PMID: 22569643 Free PMC article. Review. - Mechanism and regulation of cellular zinc transport.
Sekler I, Sensi SL, Hershfinkel M, Silverman WF. Sekler I, et al. Mol Med. 2007 Jul-Aug;13(7-8):337-43. doi: 10.2119/2007–00037.Sekler. Mol Med. 2007. PMID: 17622322 Free PMC article. Review. - Golgi Metal Ion Homeostasis in Human Health and Diseases.
Li J, Wang Y. Li J, et al. Cells. 2022 Jan 15;11(2):289. doi: 10.3390/cells11020289. Cells. 2022. PMID: 35053405 Free PMC article. Review. - Cooperative functions of ZnT1, metallothionein and ZnT4 in the cytoplasm are required for full activation of TNAP in the early secretory pathway.
Fujimoto S, Itsumura N, Tsuji T, Anan Y, Tsuji N, Ogra Y, Kimura T, Miyamae Y, Masuda S, Nagao M, Kambe T. Fujimoto S, et al. PLoS One. 2013 Oct 18;8(10):e77445. doi: 10.1371/journal.pone.0077445. eCollection 2013. PLoS One. 2013. PMID: 24204829 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous