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Driscoll, S.

Publications and source records attributed to Driscoll, S..

2 recordsLinked to original sources

A temperature-controlled, circular maintenance system for studying growth and development of pelagic tunicates (Salps)

Salps are pelagic tunicates that are able to form large blooms under favorable conditions by alternating between sexual and asexual reproduction. While their role in the regional carbon cycle is receiving attention, our knowledge of their physiology is still limited. This knowledge gap is mainly due to their fragile gelatinous nature, which makes it difficult to capture intact specimens and maintain them in the laboratory. We present here a modified kreisel tank system, that was tested onboard using the Southern Ocean salp Salpa thompsoni and station-based using the Mediterranean species Salpa fusiformis. Successful maintenance over days to weeks allowed us to obtain comparable relative growth and developmental rates as in situ, and provided insight into their potential life cycle strategies. By providing a starting point for successful maintenance, we hope to stimulate future experimental research on this understudied taxonomic group.

physiology↗

Mitf is a Schwann Cell Sensor of Axonal Integrity that Drives Nerve Repair

Schwann cells respond to acute axon damage by transiently transdifferentiating into specialized repair cells that restore sensorimotor function. However, the molecular systems controlling repair cell formation and function are not well defined and consequently it is unclear whether this form of cellular plasticity has a role in peripheral neuropathies. Here we identify Mitf as a transcriptional sensor of axon damage under the control of Nrg-ErbB-PI3K-PI5K-mTorc2 signaling. Mitf regulates a core transcriptional program for generating functional repair Schwann cells following injury and during peripheral neuropathies caused by CMT4J and CMT4D. In the absence of Mitf, core genes for epithelial-to-mesenchymal transition, metabolism and dedifferentiation are misexpressed and nerve repair is disrupted. Taken together, our findings demonstrate that Schwann cells monitor axonal health using a phosphoinositide signaling system that controls Mitf, which is critical for activating cellular plasticity and counteracting neural disease. HighlightsO_LIMitf-induced Schwann cell plasticity is triggered by peripheral neuropathy. C_LIO_LINrg-ErbB signaling activates Mitf via cytoplasmic-to-nuclear translocation. C_LIO_LIMitf restores sensorimotor function following axonal breakdown. C_LIO_LIMitf regulates a core repair program across both injury and neurodegeneration. C_LI

neuroscience↗