Lysosomes are the control centers for the metabolism of cells and tissues, including the brain. They break down defective proteins and other macromolecules into their basic building blocks. At the same time, they determine whether a cell grows or switches into an energy-saving mode. In doing so, they play a key role in health and disease.<\/p>\n
A research team led by Prof. Dr. Markus Damme of Bielefeld University\u00a0and Prof. Volker Haucke, Director of the\u00a0Leibniz-Forschungsinstitut f\u00fcr Molekulare Pharmakologie (FMP), has now jointly elucidated a key mechanism underlying this regulation. \u201cFor the first time, we\u2019re showing which protein turns off the central transport switch ARL8B,\u201d says biochemist Markus Damme, who was recently appointed to Bielefeld University from Kiel. \u201cThis gives us a better understanding of how cells spatially organize their recycling centers\u2014or, more specifically, their sustainability centers\u2014and adapt them to nutrient deprivation,\u201d adds Prof. Volker Haucke, who is the co-last author of the study alongside Markus Damme.<\/p>\n
At the heart of this work, which was carried out through close collaboration between the teams led by Prof. Volker Haucke in Berlin and Prof. Markus Damme in Bielefeld, as well as researchers at Christian-Albrechts-Universit\u00e4t Kiel (CAU), is the protein ARL8B. It acts like a motor starter: when active, lysosomes travel along a cellular rail network\u2014known as microtubules\u2014to the cell periphery. There, they promote growth processes. Until now, however, it was unclear how this switch is turned off again.<\/p>\n
A newly discovered counterpart<\/p>\n
The Bielefeld researchers identified the protein TBC1D9B as the crucial \u201coff switch.\u201d TBC1D9B binds to the lysosomal membrane protein TMEM55B and specifically inactivates ARL8B. Experts refer to this as a GAP function (GTPase\u2011activating protein), a mechanism that returns molecular switches to their inactive state.<\/p>\n
\u201cWhen TBC1D9B or its partner TMEM55B is missing, lysosomes lose their organized positioning. They spread uncontrollably throughout the cell,\u201d explains doctoral researcher Valentin Duhay from CAU Kiel, co-first author of the study. This becomes particularly dramatic under nutrient deprivation: \u201cNormally, lysosomes then move toward the center of the cell and boost the degradation process\u2014the so-called autophagy, a kind of cellular self-cleaning. Without the newly discovered regulator, this adaptation does not work,\u201d adds FMP researcher and co-first author Dr. Miaomiao Tian.<\/p>\n
Relevance for medicine and society<\/p>\n
The study combines state\u2011of\u2011the\u2011art proteomics, genome editing, and high\u2011resolution microscopy. It demonstrates in unprecedented detail that not only the presence but also the precise positioning of lysosomes determines their function.<\/p>\n
Lysosomal dysfunction plays a key role in Alzheimer\u2019s disease, Parkinson\u2019s disease, inherited metabolic storage disorders, and cancer. When lysosomes are impaired in their regulatory and recycling functions, harmful protein deposits accumulate, for example in the brain, or tumor cells exploit these systems for their own growth.<\/p>\n
Statement by Professor Damme and Professor Haucke<\/p>\n
\u201cOur findings provide the missing piece of the puzzle regarding the regulation of ARL8B. This discovery opens up new avenues for specifically influencing pathological processes such as tumor growth,\u201d said Professor Dr. Markus Damme on the subject. Prof. Volker Haucke adds: \u201cBy specifically intervening in the signaling processes at the lysosome, we could, for example, make nerve cells more resilient and thus prevent or delay dementia, or activate immune cells\u2014which are also dependent on ARL8\u2014to combat viruses or bacteria more effectively.\u201d<\/p>\n
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