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R01NIH · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENTNIH

Dynamics of skin sensory specialization during vertebrate organogenesis

Rasmussen, Jeffrey Philip (Contact)·University of Washington, WA·2021–2026·COMPLETED
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INSTITUTION

University of Washington, WA

PRINCIPAL INVESTIGATOR

Rasmussen, Jeffrey Philip (Contact)

FUNDING

$337K

YEAR

2021

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Abstract

PROJECT SUMMARY/ABSTRACT Organ development and function requires that neurons establish precise cellular interactions with tissue­resident support cells. For example, touch­sensing somatosensory neurons project peripheral axons to the skin, where they interact with specialized skin cell types. These specialized skin cells regulate axon development and modu­ late neuronal responses to cutaneous stimuli. Reciprocally, somatosensory neurons influence skin homeostasis. Although the anatomy of vertebrate skin is well described, little is known about the dynamic process of sensory specialization of the skin, partly because most studies have focused on mammalian embryos, which has limited access to live­imaging. The external development and the availability of unique transgenic tools make zebrafish an ideal model for study­ ing the dynamics of neuron and tissue maturation. This proposal investigates the development of a novel popula­ tion of specialized sensory cells that we identified in the zebrafish epidermis. Preliminary cellular, molecular and developmental analyses suggest that these zebrafish epidermal cells are the equivalent of mammalian Merkel cells, specialized mechanosensory cells that detect touch. The experiments proposed here investigate how de­ velopment of these specialized epidermal cells is coordinated with skin and nervous system maturation. In Aim 1, we will use live­imaging and genetic manipulation to characterize how sensory cell addition occurs during skin growth. Aim 2 investigates the establishment of interactions between axons and epidermal cells and how neurons promote skin specialization. Finally, in Aim 3, we will use in vivo photoconversion, lineage tracing and molecular techniques to track the trajectory of skin­resident stem cells as they differentiate into sensory cells. Collectively, these studies will provide mechanistic insights into organ specialization during development, interactions between peripheral axons and their target tissues, and potentially point to the origins of touch­sensing disorders.

R01EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENTDevelopment - 1 Study Section[DEV1]requiresabouttypesneuronsaccessadditionresponsesdescribedtargetzebrafishvertebratesummarysfdspecializedregulategeneticduringmanipulationavailabilityvelopment

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