Department of Physiology (Cellular Physiology Research Group), Institute of Molecular Pathology Biomarkers (IMPB), Universidad de Extremadura, 10003, Caceres, Spain.
Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.
Sci Rep. 2023 Nov 9;13(1):19471. doi: 10.1038/s41598-023-46946-8.
Orai1 is the pore-forming subunit of the Ca-release activated Ca channels that mediate store-operated Ca entry (SOCE) in excitable and non-excitable cells. Two Orai1 forms have been identified in mammalian cells, the full-length variant Orai1α, and the short form Orai1β, lacking the N-terminal 63 amino acids. Stem cells were isolated from non-tumoral breast epithelial cells of the MCF10A cell line, and the most representative ER+ , HER2 or triple negative breast cancer cell lines MCF7, SKBR3 and MDA-MB-231, respectively. Orai and TRPC family members expression was detected by RT-PCR and Western blotting. Changes in cytosolic Ca concentration were analyzed by confocal microscopy using Fluo 4 and the spheroid-forming ability and self-renewal was estimated in culture plates coated with pHEMA using a cell imaging system. Here, we have characterized the expression of Orai family members and several TRPC channels at the transcript level in breast stem cells (BSC) derived from the non-tumoral breast epithelial cell line MCF10A and breast cancer stem cells (BCSC) derived from the well-known estrogen receptor positive (ER+), HER2 and triple negative cell lines MCF7, SKBR3 and MDA-MB-231, respectively. Furthermore, we have evaluated the mammosphere formation efficiency and self-renewal of the BSC and BCSC. Next, through a combination of Orai1 knockdown by iRNA and the use of MDA-MB-231 KO cells, missing the native Orai1, transfected with plasmids encoding for either Orai1α or Orai1β, we show that Orai1 is essential for mammosphere formation and self-renewal efficiency in BCSC derived from triple negative and HER2 subtypes cell cultures, while this channel has a negligible effect in BCSC derived from ER+ cells as well as in non-tumoral BSC. Both, Orai1α, and Orai1β support SOCE in MDA-MB-231-derived BCSC with similar efficiency, as well as COX activation and mammosphere formation. These findings provide evidence of the functional role of Orai1α and Orai1β in spheroid forming efficiency and self-renewal in breast cancer stem cells.
Orai1 是钙释放激活钙通道的孔形成亚基,在可兴奋和非兴奋细胞中介导钙库操纵性钙内流 (SOCE)。哺乳动物细胞中已经鉴定出两种 Orai1 形式,全长变体 Orai1α 和缺乏 N 端 63 个氨基酸的短形式 Orai1β。干细胞从 MCF10A 细胞系的非肿瘤性乳腺上皮细胞中分离出来,并且分别是最具代表性的 ER+、HER2 或三阴性乳腺癌细胞系 MCF7、SKBR3 和 MDA-MB-231。通过 RT-PCR 和 Western blot 检测 Orai 和 TRPC 家族成员的表达。通过共聚焦显微镜使用 Fluo 4 分析细胞质 Ca 浓度的变化,并使用细胞成像系统在涂有 pHEMA 的培养板上估计球体形成能力和自我更新。在这里,我们已经在源自非肿瘤性乳腺上皮细胞系 MCF10A 的乳腺干细胞 (BSC) 和源自著名雌激素受体阳性 (ER+)、HER2 和三阴性细胞系 MCF7、SKBR3 和 MDA-MB-231 的乳腺癌干细胞 (BCSC) 中在转录水平上表征了 Orai 家族成员和几种 TRPC 通道的表达。此外,我们评估了 BSC 和 BCSC 的类器官形成效率和自我更新。接下来,通过 iRNA 敲低 Orai1 和使用缺失天然 Orai1 的 MDA-MB-231 KO 细胞,转染编码 Orai1α 或 Orai1β 的质粒,我们表明 Orai1 对于源自三阴性和 HER2 亚型细胞培养物的 BCSC 的类器官形成和自我更新效率是必不可少的,而这种通道对源自 ER+细胞的 BCSC 以及非肿瘤性 BSC 的影响可以忽略不计。Orai1α 和 Orai1β 以相似的效率支持源自 MDA-MB-231 的 BCSC 中的 SOCE,以及 COX 激活和类器官形成。这些发现为 Orai1α 和 Orai1β 在乳腺癌干细胞球体形成效率和自我更新中的功能作用提供了证据。