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Biochim Biophys Acta Mol Cell Res. 2018 Jun;1865(6):855-862. doi: 10.1016/j.bbamcr.2018.03.007. Epub 2018 Mar 17.

Store-independent coupling between the Secretory Pathway Ca2+ transport ATPase SPCA1 and Orai1 in Golgi stress and Hailey-Hailey disease.

Author information

1
Laboratory of Cellular Transport Systems, Department of Cellular and Molecular Medicine, KU Leuven, Belgium.
2
Laboratory of Ion Channel Research, Department of Cellular and Molecular Medicine, KU Leuven, Belgium; VIB Center for Brain & Disease Research, Leuven, Belgium.
3
Laboratory of Cellular Transport Systems, Department of Cellular and Molecular Medicine, KU Leuven, Belgium. Electronic address: peter.vangheluwe@kuleuven.be.

Abstract

The Secretory Pathway Ca2+ ATPases SPCA1 and SPCA2 transport Ca2+ and Mn2+ into the Golgi and Secretory Pathway. SPCA2 mediates store-independent Ca2+ entry (SICE) via STIM1-independent activation of Orai1, inducing constitutive Ca2+ influx in mammary epithelial cells during lactation. Here, we show that like SPCA2, also the overexpression of the ubiquitous SPCA1 induces cytosolic Ca2+ influx, which is abolished by Orai1 knockdown and occurs independently of STIM1. This process elevates the Ca2+ concentration in the cytosol and in the non-endoplasmic reticulum (ER) stores, pointing to a functional coupling between Orai1 and SPCA1. In agreement with this, we demonstrate via Total Internal Reflection Fluorescence microscopy that Orai1 and SPCA1a co-localize near the plasma membrane. Interestingly, SPCA1 overexpression also induces Golgi swelling, which coincides with translocation of the transcription factor TFE3 to the nucleus, a marker of Golgi stress. The induction of Golgi stress depends on a combination of SPCA1 activity and SICE, suggesting a role for the increased Ca2+ level in the non-ER stores. Finally, we tested whether impaired SPCA1a/Orai1 coupling may be implicated in the skin disorder Hailey-Hailey disease (HHD), which is caused by SPCA1 loss-of-function. We identified HHD-associated SPCA1a mutations that impair either the Ca2+ transport function, Orai1 activation, or both, while all mutations affect the Ca2+ content of the non-ER stores. Thus, the functional coupling between SPCA1 and Orai1 increases cytosolic and intraluminal Ca2+ levels, representing a novel mechanism of SICE that may be affected in HHD.

KEYWORDS:

Breast cancer; Calcium transport; Golgi stress response; Organelle contact site; Store operated Ca(2+) entry

PMID:
29555205
DOI:
10.1016/j.bbamcr.2018.03.007
[Indexed for MEDLINE]
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