Mechanisms of malignancy in glioblastoma cells are linked to MCU upregulation and higher intracellular calcium level

Author:

Li Xiaoyun1,Spelat Renza1,Bartolini Anna2,Cesselli Daniela23,Ius Tamara4ORCID,Skrap Miran4,Caponnetto Federica3,Manini Ivana3ORCID,Yang Yili5,Torre Vincent15ORCID

Affiliation:

1. Neurobiology Sector, International School for Advanced Studies (SISSA), Trieste, Italy

2. Institute of Pathology, University Hospital of Udine, Udine, Italy

3. Department of Medicine, University of Udine, Udine, Italy

4. Neurosurgery Unit, Department of Neurosciences, University Hospital of Udine, Udine, Italy

5. Joint SISSA-ISM Laboratory, Suzhou Institute of Systems Medicine, Chinese Academy of Medical Sciences, Suzhou, Jiangsu, China

Abstract

Glioblastoma (GBM) is one of the most malignant brain tumours, and despite advances in treatment modalities, it remains largely incurable. Calcium regulation and dynamics play crucial roles in different aspects of cancer, but they have never been investigated in detail in GBM. Here, we report that spontaneous calcium waves in GBM cells cause unusual [Ca2+]i elevations (>1 µM), often propagating through tumour microtubes (TMs) connecting adjacent cells. This unusual [Ca2+]i elevation is not associated with the induction of cell death and is concomitant with overexpression of mitochondrial calcium uniporter (MCU). Here, we show that MCU silencing decreases proliferation and alters [Ca2+]i dynamics in U87 GBM cells, while MCU overexpression increases [Ca2+]i elevation in human astrocytes (HA). These results suggest that changes in the expression level of MCU, a protein involved in intracellular calcium regulation, influences GBM cell proliferation, contributing to GBM malignancy.

Funder

Regione Autonoma Friuli Venezia Giulia

Publisher

The Company of Biologists

Subject

Cell Biology

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