# STIMULUS-RECEPTOR INTERACTION AND NEUTROPHIL RESPONSE

> **NIH NIH R01** · SCRIPPS CLINIC AND RESEARCH FOUNDATION · 1987 · $132,041

## Abstract

Neutrophils are stimulated by specific ligands that interact with distinct
classes of membrane receptors.  In response, these cells migrate,
phagocytize particles, generate injurious oxidants and discharge granule
enzymes.  These processes constitute fundamental facets of inflammation and
contribute to a variety of human diseases.  The goal of this proposed
research is to describe quantitatively how the interactions of a model
ligand, a fluorescent N-formyl peptide, with is receptor leads to the
observed cellular responses, particularly the secretion of proteases and
the production of free radicals of oxygen.  Stimulatory ligands bind to the
receptor with a half time (less than 1 minute) which is considerably longer
than the period required to initiate the cellular responses (less than 5
seconds).  The binding of the ligands appears to involve a change in
receptor affinity which occurs prior to or during the course of the
cellular response.  The observed cellular responses depend both upon the
rate and number of receptors occupied and may depend in part upon the
proportion of receptors in the available affinity states.  Internalization
of the ligand-receptor complex is slower than the cellular responses noted
above and appears to be separable, in time, from the binding events and the
change in receptor affinity.  We propose to describe in detail the
quantitative relationships among receptor occupancy, cellular responses,
and those biochemical events which initiate the cellular responses.  In
particular, we will:  1) define the interactions of stimulatory and
non-stimulatory ligands with the receptor;  2) analyze the residence
characteristics of these ligands and relate these characteristics to the
cellular responses;  3) examine the dependence of the cellular responses on
the rate and extent of receptor occupancy.  To accomplish these goals we
have available:  1) a series of novel real-time spectroscopic procedures
with which to analyze ligand binding, ligand dissociation, ligand
internalization, and cellular responses, all with a time resolution of 1 to
5 seconds;  2) methods to control independently the rate and the extent of
receptor occupancy;  3) computerized analyses of the kinetics of ligand
binding and dissociation and competitive binding interactions.  Our work
will not only yield unique information concerning the stimulation of
neutrophils but should have applicability to many related areas of
receptor-mediated cell stimulation.

## Key facts

- **NIH application ID:** 3128451
- **Project number:** 5R01AI019032-05
- **Recipient organization:** SCRIPPS CLINIC AND RESEARCH FOUNDATION
- **Principal Investigator:** LARRY A. SKLAR
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 1987
- **Award amount:** $132,041
- **Award type:** 5
- **Project period:** 1983-04-01 → 1988-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/3128451

## Citation

> US National Institutes of Health, RePORTER application 3128451, STIMULUS-RECEPTOR INTERACTION AND NEUTROPHIL RESPONSE (5R01AI019032-05). Retrieved via MORVS 2026-10-25 from https://api.morvs.ai/grant/nih/3128451. Licensed CC0.

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