Primary cilia as dynamic and diverse signalling hubs in development and disease

P Mill, ST Christensen, LB Pedersen - Nature Reviews Genetics, 2023 - nature.com
Primary cilia, antenna-like sensory organelles protruding from the surface of most vertebrate
cell types, are essential for regulating signalling pathways during development and adult …

Establishing and regulating the composition of cilia for signal transduction

MV Nachury, DU Mick - Nature reviews Molecular cell biology, 2019 - nature.com
The primary cilium is a hair-like surface-exposed organelle of the eukaryotic cell that
decodes a variety of signals—such as odorants, light and Hedgehog morphogens—by …

Merging organoid and organ-on-a-chip technology to generate complex multi-layer tissue models in a human retina-on-a-chip platform

K Achberger, C Probst, J Haderspeck, S Bolz, J Rogal… - elife, 2019 - elifesciences.org
The devastating effects and incurable nature of hereditary and sporadic retinal diseases
such as Stargardt disease, age-related macular degeneration or retinitis pigmentosa …

An actin network dispatches ciliary GPCRs into extracellular vesicles to modulate signaling

AR Nager, JS Goldstein, V Herranz-Pérez, D Portran… - Cell, 2017 - cell.com
Signaling receptors dynamically exit cilia upon activation of signaling pathways such as
Hedgehog. Here, we find that when activated G protein-coupled receptors (GPCRs) fail to …

BBSome trains remove activated GPCRs from cilia by enabling passage through the transition zone

F Ye, AR Nager, MV Nachury - Journal of Cell Biology, 2018 - rupress.org
A diffusion barrier at the transition zone enables the compartmentalization of signaling
molecules by cilia. The BBSome and the small guanosine triphosphatase Arl6, which …

The molecular machines that traffic signaling receptors into and out of cilia

MV Nachury - Current opinion in cell biology, 2018 - Elsevier
Cilia are surface-exposed organelles that dynamically concentrate signaling molecules to
organize sensory, developmental and homeostatic pathways. Entry and exit of signaling …

Trafficking of ciliary membrane proteins by the intraflagellar transport/BBSome machinery

JL Wingfield, KF Lechtreck… - Essays in biochemistry, 2018 - portlandpress.com
Bardet–Biedl syndrome (BBS) is a rare inherited disease caused by defects in the BBSome,
an octameric complex of BBS proteins. The BBSome is conserved in most organisms with …

Getting around the cell: physical transport in the intracellular world

SS Mogre, AI Brown, EF Koslover - Physical Biology, 2020 - iopscience.iop.org
Eukaryotic cells face the challenging task of transporting a variety of particles through the
complex intracellular milieu in order to deliver, distribute, and mix the many components that …

Molecular basis for photoreceptor outer segment architecture

AFX Goldberg, OL Moritz, DS Williams - Progress in retinal and eye …, 2016 - Elsevier
To serve vision, vertebrate rod and cone photoreceptors must detect photons, convert the
light stimuli into cellular signals, and then convey the encoded information to downstream …

The Bardet–Biedl syndrome protein complex is an adapter expanding the cargo range of intraflagellar transport trains for ciliary export

P Liu, KF Lechtreck - … of the National Academy of Sciences, 2018 - National Acad Sciences
Bardet–Biedl syndrome (BBS) is a ciliopathy resulting from defects in the BBSome, a
conserved protein complex. BBSome mutations affect ciliary membrane composition …