KANAZAWA, Japan, Sept. 7, 2020
KANAZAWA, Japan, Sept. 7, 2020 /PRNewswire/ -- Researchers at Kanazawa University report in Nature Communications the discovery that in the developing fly brain, neurons stemming from the same parent cell experience repulsion. This lineage-dependent repulsion is regulated by a protein known as Dscam1.
The brain's structure has columnar features, which are hypothesized to arise from nerve cells (neurons) stemming from the same parent cell, initially forming radial units. How exactly this process unfolds at the molecular level remains unexplained, however. Now, an important insight comes from Makoto Sato and colleagues from Kanazawa University who show how, in the fly brain, a gene known as Dscam regulates how neurons from one lineage repel each other, and project their axons to different columns. (Axons or nerve fibers are long protrusions of nerve cells, the function of which is to conduct electrical signals). This finding corroborates the 'radial unit hypothesis', with the mechanism at play being lineage-dependent repulsion between sister neurons.
The researchers first looked at the evolution of neuron growth in the medulla, a part of the fly's visual system featuring a columnar structure. Its development is similar to that of the cerebral cortex in the brain of mammals; it involves neuroblasts (neural stem-like cells) that produce radially oriented and clonally related groups of neurons. Sato and colleagues recorded the distances between sister neurons (i.e., neurons stemming from the same neuroblast and forming a radial unit) and between axon pairs. From the obtained distance data, the scientists were able to conclude that the sister neurons often repel each other — this observation is consistent with the formation of columns. Sato and colleagues call this process 'lineage-dependent repulsion'.
The mechanism that enables lineage-dependent repulsion must lie in daughter neurons derived from the same neuroblast 'remembering' the identity of their common mother neuroblast. Sato and colleagues put forward the explanation that the protein Dscam1 is involved. Dscam1 can develop nearly 20,000 variants, but when two identical Dscam1 molecules bind, they lead to a repulsive signal known to control self-avoidance in certain dendritic processes — dendrites are branch-like extensions of nerve cells. The reasoning then is that daughter neurons stemming from the same neuroblast produce the same Dscam1 variant, and so repel each other, whereas neurons of different lineages express different Dscam1 variants that don't repel each other and can project to the same column.
The scientists were able to support their argumentation by a series of experiments confirming the relation between Dscam1 and lineage-dependent repulsion. Sato and colleagues note that "the mechanism that we propose … is very simple", and add that it will be "interesting to determine whether similar mechanisms exist in other biological systems including column formation in mammalian brains."
Radial unit hypothesis
The radial unit hypothesis is a theory describing the development of the cerebral cortex. (The cerebral cortex is the outer layer of neural tissue of the largest part of the human brain. It plays an important role in brain functions like perception, thought, memory, language, and consciousness.) The hypothesis asserts that in the early stages of development, the cerebral cortex forms as an assembly of interacting 'columns', or 'radial units', with each unit originating from a stem cell layer containing neural stem cells. Makoto Sato and colleagues from Kanazawa University now present results showing that, in the fly brain, neurons from one lineage project their axons to different columns, and that this mechanism is regulated by the gene Dscam (Down syndrome cell adhesion molecule).
The fly Drosophila Dscam1 gene encodes more than 19,000 variants ('isoforms'). Binding of Dscam1 with identical isoforms results in a repulsive signal, which is important for certain self-avoidance mechanisms within cells. Sato and colleagues showed that in fly larvae, Dscam1 is expressed in neuroblasts, and therefore inherited by neurons having the same lineage. This results in lineage-dependent repulsion between neurons in radial units, which then plays an important role in the development of the columnar structure of the fly's medulla.
Chuyan Liu, Olena Trush, Xujun Han, Miaoxing Wang, Rie Takayama, Tetsuo Yasugi, Takashi Hayashi, and Makoto Sato. Dscam1 establishes the columnar units through lineage-dependent repulsion between sister neurons in the fly brain, Nature Communications 11, 4067 (2020).
Link to Fig.1
Caption: Dscam regulates lineage-dependent repulsion. Neurons of the same lineage repel each other and project to different columns under the control of Dscam.
Link to Fig.2
Caption: Neurons of the same lineage are labeled by the same Dscam variant and project to different columns. Neurons that derive from the same neuroblast repel each other due to the expression of the same Dscam variant (labeled in the same color), and project to different columns.
Link to Fig.3
Caption: Neurons of the same lineage project to the same column in Dscam mutant brains. Neurons of the same lineage do not repel each other in the absence of Dscam function, and project to the same column. As a result, the columns show abnormal shape.
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Institute for Frontier Science Initiative (InFiniti) was established in April 2015 for the purpose of creating innovative research results and opening new fields of scientific inquiry. The Institute enhances the academic advantages of Kanazawa University, promotes interdisciplinary research, and accelerates international circulation of talented researchers. It also cultivates young researchers' interdisciplinarity, comprehensiveness, and internationality on the basis of its research results.
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As the leading comprehensive university on the Sea of Japan coast, Kanazawa University has contributed greatly to higher education and academic research in Japan since it was founded in 1949. The University has three colleges and 17 schools offering courses in subjects that include medicine, computer engineering, and humanities.
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