Skip to main content
News Bradke 02.2023
Microscope image of a mouse brain that was genetically changed in its embryonic stage. The scientists looked at two groups of neurons: one group that only had a special dye (magenta) and another group that had a dye plus were made to express a specific peptide blocking the centrosome from forming microtubules of the cell (yellow).
© Sebastian Dupraz / DZNE

News categories: Publication

Wiring and movement of nerve cells interwoven, but controlled separately

Researchers from the DZNE have solved an important puzzle in neurobiology

As nerve cells form, they wire the brain to enable communication with other nerve cells. One of these wires, the axon, becomes long; these wires are a basis for neuronal networks. At the same time, nerve cells migrate to a specific place in the brain, the cortex. Remarkably, these dynamic processes are separately controlled: The axon continues to grow to connect with its target cells even after the nerve cell has already found its final position. "We found that the centrosome – an organelle that drives cell division - regulates the nerve cell migration; for the formation and growth of the axon, however, it does not play a role," Dr. Stanislav Vinopal and Dr. Sebastian Dupraz from the team of ImmunoSensation member Prof. Frank Bradke say. They are the first authors of the study, which now appears in the prestigious journal Neuron.

Until now, experts have debated the role of the centrosome. The process of growth and migration is enabled by a dynamic skeleton of the cell, the cytoskeleton. The cytoskeleton comprises microscopic tubules, called microtubules. They form also the backbone of the axon. The microtubules can be generated by the centrosome. With their results, the participating researchers from the group of Professor Dr. Frank Bradke have solved a central puzzle in the field of neurobiology, which science has been trying to answer for years.

The fact that the growth of the axon and the control of its migratory movement are not related is an unexpected result: "Both actions occur simultaneously and both are dependent on microtubules. And still, they are controlled independently of each other," says Stanislav Vinopal, who, after working for the DZNE, is now conducting research at Jan Evangelista Purkyne University in Usti nad Labem, Czech Republic.

For their study, the researchers developed novel molecular tools. "These molecular tools allow us to finely control the function of the centrosome to generate microtubules" explains Sebastian Dupraz. In this way, its activity can be decreased or increased. The scientists showed in the mouse brains that the axon form independently of the centrosomal activity. However, neuronal migration is significantly influenced. "A different mechanism is apparently responsible for the growth of the axon, the so-called acentrosomal formation of microtubules," concludes Dupraz: "This will now become the subject of our future research."

With their work, the scientists can now align two theories that previously contradicted each other: There were proponents of the theory that the centrosome plays a significant role in neuronal development and those who disputed it. "For our study, we disentangled the two mechanisms thatoccur in neurons simultaneously," says Stanislav Vinopal. "For the growth of the axon itself, we found that the centrosome is not necessary. For the process of neuronal migration, however, it plays a major role."

The DZNE scientists' discovery may help develop a molecular therapy for some inherited diseases, such as so-called developmental pachygyrias, that are linked to mutations of the centrosomal protein gamma-tubulin. Also in these disease phenotypes, axons are mostly intact, while neuronal migration is impaired. "Presumably, the same molecular mechanism is behind these disorders, so afuture therapy might focus on this point," the DZNE researchers say.


Publication

Stanislav Vinopal, Sebastian Dupraz et al. (2023); Centrosomal microtubule nucleation regulates radial migration of projection neurons independently of polarization in the developing brain. Neuron. DOI: 10.1016/j.neuron.2023.01.020


Contact

Sabine Hoffmann

Head of Communications and Press Spokesperson (DZNE)

sabine.hoffmann(at)dzne.de

+49 228 43302-260

Lead author Sebastian Dupraz and his publication are featured in Episode #7 of Spot on Science

Related news

Die künstlerische Abbildung zeigt Seeigel der Art Arbacia punctulata, die Spermien (weiße Wolke) und Eier (orangefarbene Wolke) ins Wasser abgeben. Von den Eiern freigesetzte Pheromone steuern die Synchronität des Laichens.

News categories: Publication

What Makes Sea Urchin and Salmon Sperm Swim

A recent study by the Max Planck Institute for Multidisciplinary Sciences and the University of Bonn shows that pH plays a crucial role in sperm motility in sea urchins and salmon. A rise in pH activates the enzyme soluble adenylyl cyclase (sAC), which produces the messenger molecule cAMP and thereby regulates sperm movement. This mechanism may be widespread in many marine invertebrates and fish. The findings have now been published in the Journal Proceedings of the National Academy of Sciences.
View entry
3 Wissenschaftler

News categories: Publication

Immune cells remember their location

A new AI-based method reconstructs spatial information about where immune cells were originally located in an organ, even after these cells have been removed from the tissue and analyzed individually. To accomplish this, Researchers at the University Hospital Bonn (UKB) and the University of Bonn use the transcriptome, i.e., the entirety of all messenger RNA transcripts produced by genes within a cell at a given time. The work has now been published in the journal Advanced Science and introduces the new MERLIN algorithm.
View entry
News Icon

News categories: Publication

B cells maintain antigen presentation in the splenic marginal zone

A team of international researchers, including ImmunoSensation³ members Prof. Niels Lemmermann and Prof. Andreas Schlitzer, shows that B cells support antiviral CD8⁺ T-cell responses beyond antibody production. In a murine CMV model, B-cell deficiency weakened virus-specific CD8⁺ T-cell responses. Mechanistically, B-cell-derived lymphotoxin β maintained CD169⁺ macrophages and Langerin⁺ cDC1 cells in the splenic marginal zone, enabling efficient T-cell priming. The study was published in Cellular & Molecular Immunology.
Full publication

Back to the news overview