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Caspase-3 cleaves extracellular vesicle proteins during auditory brainstem development

ABSTRACT: Sound localization requires extremely precise development of auditory brainstem circuits, the molecular mechanisms of which are largely unknown. We previously demonstrated a novel requirement for non-apoptotic activity of the protease caspase-3 in chick auditory brainstem development. Here, we used mass spectrometry to identify proteolytic substrates of caspase-3 during chick auditory brainstem development. Functional annotation analysis revealed that our caspase-3 substrates were enriched more than two-fold for proteins associated with extracellular vesicles (EVs), membrane-bound nanoparticles that function in intercellular communication. The proteome of EVs isolated from the auditory brainstem contained caspase-3 and was highly enriched for the caspase-3 substrates identified here. Additionally, we identified two caspase-3 substrates with known functions in axon guidance, namely Neural Cell Adhesion Molecule (NCAM) and Neuronal-glial Cell Adhesion Molecule (Ng-CAM), that were found in auditory brainstem EVs and expressed in the auditory pathway alongside cleaved caspase-3. Taken together, these data suggest a novel developmental mechanism whereby caspase-3 influences auditory brainstem circuit formation through the proteolytic cleavage of EV proteins.

INSTRUMENT(S): LTQ Orbitrap Velos

ORGANISM(S): Gallus Gallus (chicken)

TISSUE(S): Hindbrain

SUBMITTER: Forrest Weghorst

LAB HEAD: Karina Cramer

PROVIDER: PXD021728 | Pride | 2020-10-16

REPOSITORIES: Pride

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			Action	DRS
	2018-04-24-Cramer-DMSO-160.raw	Raw
	2018-04-24-Cramer-DMSO-205.raw	Raw
	2018-04-24-Cramer-DMSO-255.raw	Raw
	2018-04-24-Cramer-DMSO-325.raw	Raw
	2018-04-24-Cramer-DMSO-540.raw	Raw

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