idw – Informationsdienst Wissenschaft
Nachrichten, Termine, Experten
Nachrichten, Termine, Experten
idw - Informationsdienst
Wissenschaft
Scientists have discovered a new function of the protein tBID, which until now had only been associated with its regulatory role in cell death and cancer. However, tBID can also directly mediate controlled cell death (apoptosis). This opens up a new approach in cancer therapy / publication in ‘The EMBO Journal’
The protein tBID can trigger programmed cell death (apoptosis) by inducing damage in the energy suppliers of the cells, the mitochondria. Apoptosis is essential for maintaining tissue balance. In addition, apoptosis plays a critical role as a defence mechanism and in the elimination of damaged or redundant cells in our bodies. Impaired apoptosis has been linked to many human diseases, from cancer and autoimmune diseases to neurological disorders and heart failure. The discovery by Professor Dr Ana Garcia-Saez and her collaborators and colleagues at the University of Cologne’s CECAD Cluster of Excellence for Aging Research that tBID, previously thought to be a signal transducer, can also execute apoptosis could open up new therapies to treat malignant cells such as cancer cells. The article ‘tBID can act as a BAX-like effector of apoptosis’ has now been published in The EMBO Journal.
The protein tBID belongs to the family of BCL-2 proteins, which are fundamentally important for the self-determined apoptosis of cells and tissue balance. Because of the overlapping functions of this protein family, studying them individually is particularly challenging. Garcia-Saez and her team set out to characterize the roles of the various family members. Using cell lines lacking much of the BCL-2 proteins, they were able to determine the function of tBID. In addition, state-of-the-art microscopy (confocal, STED and electron microscopy) was used to analyse in detail the effects of tBID at the mitochondrial membrane in the cell. Activating tBID was also able to combat cellular infection with the bacterium Shigella flexneri and kill blood cancer cells (leukemia). In addition, the researchers showed that apoptosis triggered by tBID is independent of other known apoptosis induction pathways.
‘For us, it was amazing to see that proteins which are quite well known still surprise us after four decades. The realization that a protein that was considered a signal transducer for twenty years has an effector function under certain conditions is mind-blowing,’ Garcia-Saez remarked. This newly discovered function of tBID could in the future become useful in medicine. ‘For example, activating tBID could induce apoptosis when other known apoptosis signalling pathways fail or lack the proteins that carry it out,’ said Garcia-Saez. ‘Activating tBID could also help with Shigella infections, where the proteins that usually induce apoptosis are not activated.’
The work for this study started at the IFIB (Interfaculty Institute of Biochemistry) in Tübingen and was further developed at the CECAD Research Center, Institute for Genetics, in Garcia-Saez’s core laboratory, together with the laboratories of Professor Dr Hamid Kashkar und Dr Lukas Frenzel as well as external collaborators from the University of Nebraska and the laboratory of Andreas Villunger (University of Innsbruck and CeMM Research Center, Austria).
Media Contact:
Professor Dr Ana J. Garcia-Saez
+49 221 478 84263
ana.garcia@uni-koeln.de
Press and Communications Team:
Dr Anna Euteneuer
+49 221 478 84043
anna.euteneuer@uni-koeln.de
Publication:
Flores-Romero H, Hohorst L, John M, Albert MC, King LE, Beckmann L, Szabo T, Hertlein V, Luo X, Villunger A, Frenzel LP, Kashkar H and Garcia-Saez AJ. tBID can act as a BAX-like effector of apoptosis. EMBO J 2021
https://www.embopress.org/doi/10.15252/embj.2021108690
Verantwortlich: Jürgen Rees – j.rees@verw.uni-koeln.de
Merkmale dieser Pressemitteilung:
Journalisten, Studierende, Wissenschaftler
Medizin
überregional
Forschungsergebnisse, Wissenschaftliche Publikationen
Englisch
Sie können Suchbegriffe mit und, oder und / oder nicht verknüpfen, z. B. Philo nicht logie.
Verknüpfungen können Sie mit Klammern voneinander trennen, z. B. (Philo nicht logie) oder (Psycho und logie).
Zusammenhängende Worte werden als Wortgruppe gesucht, wenn Sie sie in Anführungsstriche setzen, z. B. „Bundesrepublik Deutschland“.
Die Erweiterte Suche können Sie auch nutzen, ohne Suchbegriffe einzugeben. Sie orientiert sich dann an den Kriterien, die Sie ausgewählt haben (z. B. nach dem Land oder dem Sachgebiet).
Haben Sie in einer Kategorie kein Kriterium ausgewählt, wird die gesamte Kategorie durchsucht (z.B. alle Sachgebiete oder alle Länder).
