The activation of mTor complex 1 in the cell is central to many vital processes in the body such as cell growth and metabolism. Overactivity of this signalling pathway can result in diseases such as in diabetic insulin resistance and cancer. A team led by the scientist Volker Haucke (Leibniz – Forschungsinstitut für Molekulare Pharmakologie and Freie Universität Berlin) has now discovered how inactivation of a certain lipid kinase promotes mTor complex 1 activity, and may therefore constitute a new point of attack for the treatment of diabetes and cancer. The results have just been published in the renowned journal Nature Cell Biology.

The signaling pathways in somatic cells are highly complex and specific mechanisms can only be triggered if several "switches" are "flipped" in a fixed sequence. However, given the high number of substances and substance complexes involved in the cellular signal transmission, finding these "switches" and identifying their role is a real challenge. The question of how mTor complex 1 can be deactivated in the cell has also been long unresolved. Even so, FMP researchers were able to shed light on this "switch" as early as 2017: revealing that a certain lipid kinase (PI3KC2ß) acts as a natural brake for the mTor protein and ensures that the mTor complex 1 is switched off, for example, when certain hormonal signals such as insulin are absent.

Now, a team led by FMP researcher Alexander Wallroth from Volker Haucke's research group has been scrutinizing how this lipid kinase is regulated. Alexander Wallroth: "We manipulated the lipid kinase in various ways and looked at the effects these manipulations had on mTOR and activity on cell growth". This work has allowed the researchers to uncover a mechanism for inactivating the PI3KC2ß lipid kinase. Another kinase that plays a key role here is protein kinase N (PKN), which renders the PI3KC2ß lipid kinase inactive, thereby indirectly activating mTOR in the process. Protein kinase N is regulated by growth factors that stimulate the mTor complex 2 at the cell membrane - the second protein complex in which mTor is present in the cell. This, in turn, activates PKN, which ultimately inactivates the lipid kinase.

^{Left: Protein kinase N (PKN) is active and inhibits PI3KC2ß (green).
Right: PKN is missing. This causes PI3KC2ß to change the localization in the cell and to become active.
Picture: Alexander Wallroth, FMP}

“In doing so, we revealed two further components prone to pharmacological attack“, explains Alexander Wallroth. Successfully inhibiting PKN activates the lipid kinase PI3KC2ß and ends up inhibiting mTOR-dependent cell growth. Conversely, if the signaling pathway is activated by growth factors, mTOR complex 2, and, finally, PKN, the lipid kinase remains inactive and the mTOR complex 1 is able to drive cell growth. Although inhibitors capable of inhibiting PKN have already been identified, their lack of specificity and tendency to block many other vital cellular processes currently precludes their use in living tissue.

"The most fascinating finding was the discovery of a cell biological signaling pathway that links mTor complexes 1 and 2, for example switching off 2 also impacts on 1," says Alexander Wallroth. In their previous work, the researchers were able to show that the lipid kinase PI3KC2ß, when activated, acts directly on mTor complex 1. Similarly, if PKN is activated by mTor complex 2, thereby inactivating the lipid kinase, the activity of mTor complex 1 is also affected. Up to now, little was known about mTor complex 2 compared to complex 1. The new results show that mTor complex 2 has a decisive impact on the activity of the important complex 1. "This paves the way for further and more detailed research into medical intervention to encompass various diseases such as insulin resistance or cancer," emphasizes Alexander Wallroth.

Original publications:
Marat, A.L., Wallroth, A., Lo, W., Müller, R., Norata, G.D., Falsaca, M., Schultz, C., Haucke, V. (2017) mTORC1 activity repression by late endosomal phosphatidylinositol 3,4 bisphosphate. Science, Ausgabe vom 2. Juni 2017
Wallroth, A., Koch, P. A., Marat, A. L., Krause, E., Haucke, V. (2019). Protein kinase N controls a lysosomal lipid switch to facilitate nutrient signalling via mTORC1. Nature Cell Biology, Ausgabe September 2019

Source:
Press release Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP)

Contact:
Professor Dr. Volker Haucke
Professor of Molecular Pharmacology
Freie Universität Berlin
Member of Einstein Center for Neurosciences Berlin

Director at Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP)
Robert-Rössle-Str.10
13125 Berlin, Campus Berlin-Buch
E-Mail: haucke(at)fmp-berlin.de 
www.leibniz-fmp.de/haucke