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December 20, 2016

An “IRBIT”uary before cell death

Billions of cells in our bodies die every day in an important process called apoptosis. Now, researchers at the RIKEN Brain Science Institute have mapped out a sequence of events that are necessary for apoptosis to occur properly. Published in eLife, the study focuses on the protein IRBIT and how its action near mitochondria in our cells can set off a chain reaction that leads to programmed cell death.

Disruptions in proper apoptosis can lead to serious medical consequences. As team leader Katsuhiko Mikoshiba explains, “Excessive apoptosis in the brain is associated with several neurodegenerative diseases, while impaired apoptosis is related to some cancers and tumor formation.”

Events that happen inside our cells are often controlled by interactions between proteins and modifications of proteins that change how they can interact with each other. Mikoshiba and his team have already shown that apoptosis in neurons can be initiated when certain proteins binds to IP3 receptors. In their new study, the team investigated IRBIT, another protein commonly found in the brain that can bind to the IP3 receptor.

In a series of studies, the researchers showed that the presence of IRBIT promoted normal apoptosis. “We were actually quite surprised,” notes first author Benjamin Bonneau. “We initially expected that IRBIT would function to suppress cell death.”

The reason for this prediction was that IRBIT has been primarily described as a protein that reduces cellular calcium levels, a phenomenon that can lead to cell death. Additionally, IRBIT is located in the same parts of the body—including the developing nervous system—as Bcl2l10, another protein that is known to reduce apoptosis and which also binds to the same region of the IP3 receptor as IRBIT. The key factor in this process is the flow of calcium ions between two organelles within a cell—the ER and mitochondria. When Bcl2l10 is attached to the IP3 receptor located in the ER membrane, it reduces the flow of calcium into the mitochondria, which prevents apoptosis.

In their new study, the team first showed that IRBIT and Bcl2l10 naturally attach to different places on the IP3 receptor, and that they attach to each other. This is why they initially thought that they work together to prevent apoptosis. However, further testing revealed an important event that always preceded apoptosis—IRBIT loses a phosphate group. Protein function is often altered through small additions or subtractions. The team showed that in this case, the loss of the phosphate group prevents IRBIT from staying attached to the IP3 receptor. Instead it moves away from the ER, and drags Bcl2l10 with it. When this happens, the team saw that without Bcl2l10, calcium flow into the mitochondria increased, which led to cell death.

Understanding IRBIT’s role in facilitating apoptosis has implications for treating cancer that is associated with low levels of IRBIT expression. Bonneau notes that, “Because reduced IRBIT expression may contribute to tumor formation, the next step is to determine to what extent modulating IRBIT expression contributes to cancer formation, and if this is the case, what organs are the most sensitive.

Mikoshiba adds, “Neurodegenerative diseases such as Huntington’s disease and Parkinson’s disease are characterized by excessive apoptosis. Knowing IRBIT’s involvement gives us a new target for investigation. As IRBIT is highly expressed in the brain, the chances are good that we will be able to find a connection, which could lead to new treatment possibilities.”

Reference

  • Benjamin Bonneau, Hideaki Ando, Katsuhiro Kawaai, Matsumi Hirose, Hiromi Takahashi-Iwanaga, Katsuhiko Mikoshiba, "IRBIT controls apoptosis by interacting with the Bcl-2 homolog, Bcl2l10, and by promoting ER-mitochondria contact", eLife, doi: 10.7554/eLife19896

Contact

Laboratory Head
Katsuhiko Mikoshiba
Laboratory for Developmental Neurobiology
RIKEN Brain Science Institute

Adam Phillips
RIKEN International Affairs Division
Tel: +81-(0)48-462-1225 / Fax: +81-(0)48-463-3687
Email: pr@riken.jp

Schematic model depicting the role of IRBIT-Bcl2l10 interplay in physiological and stress conditions.

In physiological condition, in WT cells, IRBIT promotes ER-mitochondria contact rendering Ca2+ transfer easier between the two organelles. The additive effect of Bcl2l10 and phosphorylated IRBIT on IP3R maintains Ca2+ transfer to a low level. In IRBIT KO cells, although Ca2+ released through IP3R is increased due to absence of IRBIT, Ca2+ transfer to the mitochondria is reduced because of the great reduction of ER-mitochondria contact. Following an apoptotic stimuli, Ca2+ release from the ER is increased. In WT cells, IRBIT dephosphorylation induces its translocation together with Bcl2l10 allowing a massive Ca2+ transfer from ER to mitochondria. On contrary, in IRBIT KO cells, Bcl2l10 is no longer displaced from MAMs what reduces Ca2+ release from ER. This, combined to the reduction of ER-mitochondria contact, prevents massive Ca2+ transfer to mitochondria and then greatly attenuates apoptosis.