Photoreceptor discs form through peripherin-dependent suppression of ciliary ectosome release.

Published

Journal Article

The primary cilium is a highly conserved organelle housing specialized molecules responsible for receiving and processing extracellular signals. A recently discovered property shared across many cilia is the ability to release small vesicles called ectosomes, which are used for exchanging protein and genetic material among cells. In this study, we report a novel role for ciliary ectosomes in building the elaborate photoreceptor outer segment filled with hundreds of tightly packed "disc" membranes. We demonstrate that the photoreceptor cilium has an innate ability to release massive amounts of ectosomes. However, this process is suppressed by the disc-specific protein peripherin, which enables retained ectosomes to be morphed into discs. This new function of peripherin is performed independently from its well-established role in maintaining the high curvature of disc edges, and each function is fulfilled by a separate part of peripherin's molecule. Our findings explain how the outer segment structure evolved from the primary cilium to provide photoreceptor cells with vast membrane surfaces for efficient light capture.

Full Text

Duke Authors

Cited Authors

  • Salinas, RY; Pearring, JN; Ding, J-D; Spencer, WJ; Hao, Y; Arshavsky, VY

Published Date

  • May 1, 2017

Published In

Volume / Issue

  • 216 / 5

Start / End Page

  • 1489 - 1499

PubMed ID

  • 28381413

Pubmed Central ID

  • 28381413

Electronic International Standard Serial Number (EISSN)

  • 1540-8140

Digital Object Identifier (DOI)

  • 10.1083/jcb.201608081

Language

  • eng

Conference Location

  • United States