Bending Primary Cilia: evidence for a structure-function relationship? ?How do cells sense their environment?? is a question that had dominated biology for decades. Until recently, that question was answered in terms of chemical sensing via transmembrane receptors. It has become increasingly evident that cells also sense and respond to mechanical forces using a variety of sensors. The primary cilium is hypothesized to be a mechanical sensor that senses fluid flow, with the proposed mechanism being ciliary bending. However, confirming or rejecting this ?ciliary hypothesis? has proved to be difficult. One reason is that fluid flow exerts shear stress on the entire cell surface, complicating experiments designed to determine the site of fluid flow sensing. The goal of this project is to use live cell imaging and optical trapping to apply a well-controlled force localized to a single experimenter-chosen cilium and determine the minimum amount of ciliary bending, due to flow, associated with increased cytosolic Ca2+, a well-established cellular read-out of flow stimulation. Broadly, this proposal will characterize, alter, and correlate cilium mechanical properties (?stiffness?, length) with the minimum amount of flow associated with increased cytosolic Ca2+ (?threshold flow?). This project is an important first step in understanding the interplay between mechanosensation and homeostasis. Information gained during the course of this project relating mechanical properties of the cilium to activation of a signaling pathway may enable new therapeutic approaches to ciliopathies.

Public Health Relevance

Bending Primary Cilia: evidence for a structure-function relationship? We propose to measure the amount of ciliary bending that is associated with increased cytosolic Ca2+. Our proposed studies will clarify the hypothesized flow-sensing function of primary cilia. The ubiquitous existence of both primary cilium and fluid flow in other physiological systems ensures the results and conclusions will be broadly applicable and directly relevant to better understand the large class of disorders known as ciliopathies.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15GM132829-01
Application #
9728152
Study Section
Development - 2 Study Section (DEV2)
Program Officer
Ainsztein, Alexandra M
Project Start
2019-09-15
Project End
2022-08-31
Budget Start
2019-09-15
Budget End
2022-08-31
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Cleveland State University
Department
Genetics
Type
Schools of Arts and Sciences
DUNS #
010841617
City
Cleveland
State
OH
Country
United States
Zip Code
44115