4.8 Article

Stac protein regulates release of neuropeptides

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2009224117

Keywords

stac; neuropeptide; L-type voltage-gated calcium channel; Drosophila melanogaster

Funding

  1. National Institute of Arthritis and Musculoskeletal and Skin Diseases Grant [R01 AR063056]
  2. National Institute of Neurological Disorders and Stroke (NINDS) Grant [RO1 NS069844, RO1 NS032385]
  3. Rackham International Student Fellowship from the University of Michigan
  4. Rackham Barbour Scholarship from the University of Michigan
  5. Rackham Predoctoral Fellowship from the University of Michigan
  6. Rackham Research Grant from the University of Michigan
  7. Rackham One-Term Fellowship from the University of Michigan
  8. Rackham Merit Fellowship from the University of Michigan
  9. National Institute of General Medical Sciences Grant [T32 GM007315]
  10. University of Michigan

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Neuropeptides are important for regulating numerous neural functions and behaviors. Release of neuropeptides requires long-lasting, high levels of cytosolic Ca2+. However, the molecular regulation of neuropeptide release remains to be clarified. Recently, Stac3 was identified as a key regulator of L-type Ca2+ channels (CaChs) and excitation-contraction coupling in vertebrate skeletal muscles. There is a small family of stac genes in vertebrates with other members expressed by subsets of neurons in the central nervous system. The function of neural Stac proteins, however, is poorly understood. Drosophila melanogaster contain a single stac gene, Dstac, which is expressed by muscles and a subset of neurons, including neuropeptide-expressing motor neurons. Here, genetic manipulations, coupled with immunolabeling, Ca2+ imaging, electrophysiology, and behavioral analysis, revealed that Dstac regulates L-type CaChs (Dmca1D) in Drosophila motor neurons and this, in turn, controls the release of neuropeptides.

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