Patterning dendritic branches with environmental and neuronal surface molecules

NIH RePORTER · NIH · R01 · $340,040 · view on reporter.nih.gov ↗

Abstract

In this grant, we propose to understand the molecular mechanisms of dendrite morphogenesis and function. Dendrite morphogenesis determines the connectivity of neurons. We are using a model cell (PVD in C elegans) to study this question. PVD is a proprioceptive neuron that senses muscle contraction and regulates animal movement. In our previous work, we identified the extracellular ligands and their receptor on PVD that guide the dendrite growth and branching. Here, we propose to understand how the receptor-ligand interaction triggers signaling mechanisms and leads to cytoskeletal modifications which eventually drives the morphogenesis events. We will also study how the neurons regulate receptor signaling using a drug target protein called KPC-1 to control guidance decisions. We will also understand how the PVD neurons sense muscle contraction using a putative mechanosensitive channel and how it regulates neuromuscular activity through a surprising neural circuit feedback mechanism. Through these experiments, we will gain insights in the molecular logic of dendrite development. We will identify novel mechanosensitive channels that are important for body movement regulation.

Key facts

NIH application ID
9767867
Project number
5R01NS082208-07
Recipient
STANFORD UNIVERSITY
Principal Investigator
Tim Stearns
Activity code
R01
Funding institute
NIH
Fiscal year
2021
Award amount
$340,040
Award type
5
Project period
2013-06-01 → 2024-11-30