Saturday, July 5, 2025 7/5/2025

The acute effects of snake venom CRiSP toxins on blood and lymphatic endothelial cell permeability: new insights into the pathophysiology of snakebite

Award Number: R15HL137134
ORGANIZATION: NATIONAL HEART, LUNG, & BLOOD INSTITUTE
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)
PERIOD OF PERFORMANCE START DATE: 04/01/2020
PERIOD OF PERFORMANCE END DATE: 03/31/2023

Group Awards By:

View Award Description

The acute effects of snake venom CRiSP toxins on blood and lymphatic endothelial cell permeability: new insights into the pathophysiology of snakebite - PROJECT SUMMARY The overall goal of this project is to engage undergraduate and graduate students in innovative studies in molecular toxinology, studies that have the potential to contribute to important advances in our understanding of the pathophysiology of snakebite. Snakebite is a substantial global health problem, causing severe injury to 2.7 million people and claiming an estimated 125,000 deaths annually. In spite of its importance as a global health issue, very little is known on the pathophysiology of snakebite. The goal of this project is to understand the effects of snake venom Cysteine-Rich Secretory Proteins (svCRiSPs) on vascular biology and the possible role that these effects may play in the pathophysiology of snakebite. The data generated from our previous award (R15HL137134-01) has demonstrated that svCRiSP toxins have an acute effect on vascular permeability. In the forthcoming grant period, we will build upon our previous studies with student-led projects to characterize the comparative vascular activity of multiple svCRiSPs isolated from the venoms of North American snakes housed in the NNTRC. In addition we will pursue our recent discovery that extracellular vesicles (EVs) isolated from the plasma of envenomated mice contain snake venom proteins including, prominently svCRiSPs. This new finding raises the possibility that venom proteins are transported in the systemic circulation by membrane vesicle trafficking. svCRiSP EVs may play in important role in regulating immune system activity impacting vascular permeability, pro-inflammatory responses, and the progression of physiological effects in snakebite. To test our hypothesis we will address three distinct but complementary Specific Aims: Specific Aim 1: To determine the role of exosomal CRiSPs in the pathophysiology of snakebite by comparing the distribution of exosomal CRiSPs in crotaline snake envenomation and evaluate the functional vascular effect of EVs from mice treated with svCRiSPs. Specific Aim 2: to characterize the effects of Css-CRiSP on the induction of pro-inflammatory responses in vitro and in vivo. Specific Aim 3: to profile the vascular effects, molecular mechanisms, and targets of crotaline svCRiSPs prepared from additional medically significant species of North American vipers. The proposed studies will support the educational goals of our program by providing undergraduate and graduate students with hands-on research experiences that will provide an introduction to the opportunities available for careers in biomedical research. This research program will also enhance the academic environment of our university by promoting an important program of global health research. Knowledge gained from these studies will generate a more detailed understanding of the effects of svCRiSPs on vascular biology and provide a better understanding of the role svCRiSPs play in the pathophysiology of snakebite.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2024 ( Subtotal = $0 )
2024	2020	TEXAS A & M UNIVERSITY KINGSVILLE	700 N UNIVERSITY BLVD	KINGSVILLE	TX	78363	KLEBERG	USA	Blood Diseases and Resources Research	000	2	12/19/2023	COMPETING CONTINUATION	$0
														Subtotal = $0

Issue Date FY: 2021 ( Subtotal = $0 )
2021	2017	TEXAS A & M UNIVERSITY KINGSVILLE	700 UNIVERSITY BLVD	KINGSVILLE	TX	78363	KLEBERG	USA	Blood Diseases and Resources Research	000	1	6/18/2021	NEW	$0
														Subtotal = $0

Issue Date FY: 2020 ( Subtotal = $413,738 )
2020	2020	TEXAS A & M UNIVERSITY KINGSVILLE	700 UNIVERSITY BLVD	KINGSVILLE	TX	78363	KLEBERG	USA	Blood Diseases and Resources Research	000	2	3/23/2020	COMPETING CONTINUATION	$413,738
														Subtotal = $413,738

Issue Date FY: 2017 ( Subtotal = $412,734 )
2017	2017	TEXAS A & M UNIVERSITY KINGSVILLE	700 UNIVERSITY BLVD	KINGSVILLE	TX	78363	KLEBERG	USA	Blood Diseases and Resources Research	000	1	3/31/2017	NEW	$412,734
														Subtotal = $412,734

Grand Total All Awards = $826,472

Top

All Categories

About

Search

Reports

Data Submission

Award Information

The acute effects of snake venom CRiSP toxins on blood and lymphatic endothelial cell permeability: new insights into the pathophysiology of snakebite

Award Number: R15HL137134

ORGANIZATION: NATIONAL HEART, LUNG, & BLOOD INSTITUTE

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

PERIOD OF PERFORMANCE START DATE: 04/01/2020

PERIOD OF PERFORMANCE END DATE: 03/31/2023

Federal Websites

Department of Health & Human Services

HHS Operating Divisions

HHS Staff Divisions

Download A Document Viewer