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Swayne lab uses innovative live cell microscopy to get a "closer look" at the development of nerve cell connections
Pictured: Authors of the recent Dr. Swayne lab paper, clockwise from top left: Becca Candlish, Leigh Anne Swayne, Emma van der Slagt and Juan C. Sanchez-Arias
In a new paper published in eNeuro, DMCBH researcher Dr. Leigh Anne Swayne's team offers new insights that could help us understand how the pannexin 1 (PANX1) channel protein regulates the formation of nerve cell connections, a key step in brain development.
The study was led by postdoctoral fellow Dr. Juan C. Sanchez-Arias with the goal of determing whether PANX1 affected the density of nerve cell connections by regulating their formation or stability. Sanchez-Arias focused his analysis on an earlier step in nerve cell development when “young” nerve cell projections called dendritic protrusions are most abundant. These dendritic protrusions reach out to probe their environments like microscopic fingers to eventually form connections with other nerve cells.
To measure the movement of dendritic protrusions in real-time, Dr. Swayne's team used live cell confocal microscopy along with a novel approach that enhanced their detection.
The team found that dendritic protrusion stability was inversely linked to the levels of the PANX1 protein. The protrusions were more dynamic when there was more PANX1 and more stable when there was less. This suggests that PANX1 regulates dendritic spine density in part through controlling their stability in the early stages of nerve cell connection formation.
The new paper expands on a recent discovery from the Swayne lab that the PANX1 protein regulates how many connections are made between nerve cells. PANX1 is a channel protein, meaning that it forms doorways in cell membranes. PANX1 channels – a major focus of Swayne lab research – transmit signals to tell the cell how to change in response to its environment.
This story was originally published on the University of Victoria Medical Sciences Website. You can find it here.
Funding: This work was supported by operating grants from the Canadian Institutes of Health Research (MOP142215), from the Natural Sciences and Engineering Research Council (RGPIN-2017-03889), The Scottish Rite Charitable Foundation of Canada (15118) and the University of Victoria-Division of Medical Sciences to L.A.S. L.A.S. was also supported by a Michael Smith Foundation for Health Research and British Columbia Schizophrenia Society Foundation Scholar Award (5900). J.C.S.A. was supported by a University of Victoria Fellowship Graduate Award. L.A.S. is also grateful for infrastructure support from the Canada Foundation for Innovation (29462) and the BC Knowledge Development Fund (804754) for the Leica SP8 microscope system.