The distinct role of STIM1 and STIM2 in the regulation of store-operated Ca2+ entry and cellular function

Yih Fung Chen, Li Hsien Chen, Meng-Ru Shen

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Stromal interaction molecules STIM1 and STIM2 are endoplasmic reticulum (ER) Ca2+ sensors that initiate store-operated Ca 2+ entry (SOCE). The roles of STIM1-mediated SOCE in cancer biology have been highlighted in different types of cancer, but that of STIM2 is unknown. By the model of cervical cancer, here we focus on the cooperative regulation of SOCE by STIM proteins and their distinct roles in cellular function. Immunofluorescent stainings of surgical specimens of cervical cancer show that STIM1 and STIM2 are abundant in tumor tissues, but STIM1 is the major ER Ca 2+ sensor identified in the invasive front of cancer tissues. STIM1 or STIM2 overexpression in cervical cancer SiHa cells induces an upregulated SOCE. Regarding cellular function, STIM1 and STIM2 are necessary for cell proliferation, whereas STIM1 is the dominant ER Ca 2+ sensor involved in cell migration. During SOCE, STIM1 is aggregated and translocated towards the Orai1-containing plasma membrane in association with the microtubule plus-end binding protein EB1. In contrast, STIM2 is constitutively aggregated without significant trafficking or association with microtubules. These results show the distinct role of STIM1 and STIM2 in SOCE and cellular function of cervical cancer cells.

Original languageEnglish
Pages (from-to)8727-8739
Number of pages13
JournalJournal of Cellular Physiology
Volume234
Issue number6
DOIs
Publication statusPublished - 2019 Jun 1

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Uterine Cervical Neoplasms
Endoplasmic Reticulum
Sensors
Microtubules
Tissue
Neoplasms
Cell proliferation
Cell membranes
Tumors
Carrier Proteins
Cells
Cell Movement
Molecules
Cell Proliferation
Cell Membrane
Staining and Labeling
Proteins

All Science Journal Classification (ASJC) codes

  • Physiology
  • Clinical Biochemistry
  • Cell Biology

Cite this

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abstract = "Stromal interaction molecules STIM1 and STIM2 are endoplasmic reticulum (ER) Ca2+ sensors that initiate store-operated Ca 2+ entry (SOCE). The roles of STIM1-mediated SOCE in cancer biology have been highlighted in different types of cancer, but that of STIM2 is unknown. By the model of cervical cancer, here we focus on the cooperative regulation of SOCE by STIM proteins and their distinct roles in cellular function. Immunofluorescent stainings of surgical specimens of cervical cancer show that STIM1 and STIM2 are abundant in tumor tissues, but STIM1 is the major ER Ca 2+ sensor identified in the invasive front of cancer tissues. STIM1 or STIM2 overexpression in cervical cancer SiHa cells induces an upregulated SOCE. Regarding cellular function, STIM1 and STIM2 are necessary for cell proliferation, whereas STIM1 is the dominant ER Ca 2+ sensor involved in cell migration. During SOCE, STIM1 is aggregated and translocated towards the Orai1-containing plasma membrane in association with the microtubule plus-end binding protein EB1. In contrast, STIM2 is constitutively aggregated without significant trafficking or association with microtubules. These results show the distinct role of STIM1 and STIM2 in SOCE and cellular function of cervical cancer cells.",
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The distinct role of STIM1 and STIM2 in the regulation of store-operated Ca2+ entry and cellular function. / Chen, Yih Fung; Chen, Li Hsien; Shen, Meng-Ru.

In: Journal of Cellular Physiology, Vol. 234, No. 6, 01.06.2019, p. 8727-8739.

Research output: Contribution to journalArticle

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