# Trauma induced endothelial cell Ca2+ signaling

> **NIH NIH R00** · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · 2020 · $249,000

## Abstract

This proposal describes a 5-year program (2 years mentored, 3 years independent) for the
development of an academic career in cardiovascular disease and trauma pathophysiology research with an
emphasis on ion channel function and Ca2+ signaling pathways. Dr. Collier (the applicant) has a background in
ion channel structure and function, biochemistry, and molecular biology. He competed his doctoral training in
the Department of Molecular Physiology & Biophysics at the University of Iowa under the mentorship of Dr.
Peter Snyder. He came to the University of Vermont as Postdoctoral Associate to develop new skills in Ca2+
imaging, vascular biology, and animal models of traumatic injury to aid his transition toward becoming an
independent investigator.
 The University of Vermont (UVM) is internationally recognized for its strength in pharmacology, with
unique expertise in Ca2+ signaling, vascular biology, and trauma. Mark Nelson, Ph.D. will mentor Dr. Collier's
scientific development and transition to independence. Dr. Nelson is a recognized leader in the field of Ca2+
signaling and vascular biology. Dr. Nelson has trained numerous postdoctoral fellows and graduate students,
many of whom are now established independent investigators. Kalev Freeman, M.D., Ph.D. will co-mentor Dr.
Collier. Dr. Freeman provides unique clinical perspective and expertise in trauma pathophysiology. This
research environment maximizes the potential for Dr. Collier to establish a scientific niche from which an
academic career can be constructed. This project will facilitate continued technical, intellectual, and
professional training which will help Dr. Collier develop a unique skill set that will allow him to establish an
independent laboratory at an academic research institution of his choosing.
 Traumatic injury is a major public health problem. Trauma accounts for 37 million hospital visits and is
estimated to cost the U.S. more than $700 billion each year. Traumatic brain injury (TBI) accounts for 1.7
million hospital visits and often leaves survivors suffering from cardiovascular complications such as
hypertension, hypotension, coagulopathy, and stroke. The mechanism of these systemic complications is
unknown. It has been demonstrated that traumatic injury releases toxic intracellular components into the
systemic circulation, however, little is known about how these toxic factors affect tissue at the molecular level.
This project will elucidate the basis of persistent altered endothelial cell function in systemic arteries following
TBI, the mechanism by which trauma associated circulating factors induced endothelial cell Ca2+ signaling, and
the basis of preservation of cerebral artery function following TBI.

## Key facts

- **NIH application ID:** 9952407
- **Project number:** 5R00HL133451-04
- **Recipient organization:** UNIVERSITY OF TENNESSEE HEALTH SCI CTR
- **Principal Investigator:** Daniel Mohr Collier
- **Activity code:** R00 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $249,000
- **Award type:** 5
- **Project period:** 2016-09-15 → 2022-06-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9952407

## Citation

> US National Institutes of Health, RePORTER application 9952407, Trauma induced endothelial cell Ca2+ signaling (5R00HL133451-04). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/9952407. Licensed CC0.

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