Store-operated Ca 2+ entry (SOCE) provides a major Ca 2+ entry route in cancer cells. SOCE is mediated by the assembly of Stim and Orai proteins at endoplasmic reticulum (ER)-plasma membrane junctions upon depletion of the ER Ca 2+ store. Additionally, Stim and Orai proteins underpin constitutive Ca 2+ entry in a growing number of cancer cell types due to the partial depletion of their ER Ca 2+ reservoir. Herein, we investigated for the first time the structure and function of SOCE in primary cultures of colorectal carcinoma (CRC) established from primary tumor (pCRC) and metastatic lesions (mCRC) of human subjects. Stim1-2 and Orai1-3 transcripts were equally expressed in pCRC and mCRC cells, although Stim1 and Orai3 proteins were up-regulated in mCRC cells. The Mn 2+ -quenching technique revealed that constitutive Ca 2+ entry was significantly enhanced in pCRC cells and was inhibited by the pharmacological and genetic blockade of Stim1, Stim2, Orai1 and Orai3. The larger resting Ca 2+ influx in pCRC was associated to their lower ER Ca 2+ content as compared to mCRC cells. Pharmacological and genetic blockade of Stim1, Stim2, Orai1 and Orai3 prevented ER-dependent Ca 2+ release, thereby suggesting that constitutive SOCE maintains ER Ca 2+ levels. Nevertheless, pharmacological and genetic blockade of Stim1, Stim2, Orai1 and Orai3 did not affect CRC cell proliferation and migration. These data provide the first evidence that Stim and Orai proteins mediate constitutive Ca 2+ entry and replenish ER with Ca 2+ in primary cultures of CRC cells. However, SOCE is not a promising target to design alternative therapies for CRC.

Stim and Orai mediate constitutive Ca 2+ entry and control endoplasmic reticulum Ca 2+ refilling in primary cultures of colorectal carcinoma cells

Lucariello A.;Guerra G.;
2018-01-01

Abstract

Store-operated Ca 2+ entry (SOCE) provides a major Ca 2+ entry route in cancer cells. SOCE is mediated by the assembly of Stim and Orai proteins at endoplasmic reticulum (ER)-plasma membrane junctions upon depletion of the ER Ca 2+ store. Additionally, Stim and Orai proteins underpin constitutive Ca 2+ entry in a growing number of cancer cell types due to the partial depletion of their ER Ca 2+ reservoir. Herein, we investigated for the first time the structure and function of SOCE in primary cultures of colorectal carcinoma (CRC) established from primary tumor (pCRC) and metastatic lesions (mCRC) of human subjects. Stim1-2 and Orai1-3 transcripts were equally expressed in pCRC and mCRC cells, although Stim1 and Orai3 proteins were up-regulated in mCRC cells. The Mn 2+ -quenching technique revealed that constitutive Ca 2+ entry was significantly enhanced in pCRC cells and was inhibited by the pharmacological and genetic blockade of Stim1, Stim2, Orai1 and Orai3. The larger resting Ca 2+ influx in pCRC was associated to their lower ER Ca 2+ content as compared to mCRC cells. Pharmacological and genetic blockade of Stim1, Stim2, Orai1 and Orai3 prevented ER-dependent Ca 2+ release, thereby suggesting that constitutive SOCE maintains ER Ca 2+ levels. Nevertheless, pharmacological and genetic blockade of Stim1, Stim2, Orai1 and Orai3 did not affect CRC cell proliferation and migration. These data provide the first evidence that Stim and Orai proteins mediate constitutive Ca 2+ entry and replenish ER with Ca 2+ in primary cultures of CRC cells. However, SOCE is not a promising target to design alternative therapies for CRC.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11367/78277
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