Olan Jackson-Weaver, PhD

Assistant Professor

Adjunct of Physiology
School of Medicine
Department
Surgery
Physiology
CV
Document
Olan Jackson-Weaver, PhD

Education & Affiliations

2011: Ph.D., Biomedial Sciences, University of New Mexico, Albuquerque, New Mexico
2012: Post Doctoral, Physology, University of California, Los Angeles, California
2018: Post Doctoral, Biochemistry/Cell Biology, University of Southern California, Los Angeles, California

Areas of Expertise

Endothelial cell biology
calcium signaling
endothelial glycocalyx
hemorrhagic shock
protein arginine methylation

Biography

Dr. Olan Jackson-Weaver joined our Department of Surgery in September 2018 as a Research Assistant Professor in the Division of Trauma and Acute Care Education. He was born and raised in Albuquerqe, New Mexico. After completing his Bachelors degrees in Chemistry and Biology and his Ph.D. in Biomedical Sciences (vascular physiology focus) from the University of New Mexico, He received postdoctoral training at the University of California Los Angeles and the University of Southern California studying astrocyte calcium signaling and the roles of protein arginine methylation in heart development and disease. His lab at Tulane University studies several aspects of endothelial cell biology, including endothelial cell damage during shock and trauma and the role of Ca2+ signaling modalities in the regulation of angiogenesis.

Research

Our lab is interested in the roles of endothelial calcium signaling in hemorrhagic shock, ischemia-reperfusion injury, acute lung injury, and angiogenesis. We are currently focusing on the role of mitochondrial reactive oxygen species in regulating endothelial calcium signaling in these disease states, and how the proteoglycan surface layer of the endothelium can be damaged by this signaling mechanism. The endothelium is vital in maintaining hemodynamic, coagulation, tissue fluid, and inflammatory homeostasis. These pathways are all affected by ischemia-reperfusion events such as hemorrhagic shock and resuscitation, and thus damage to the endothelium is thought to be a fundamental pathological mechanism in these events. Therefore, exploring the mechanisms of ischemia-reperfusion signaling in endothelial cells with an eye towards therapeutic opportunities is of great importance for improving treatments of a wide variety of disease states.


The other side of the coin is the important function of endothelial calcium signaling in regulating vascular tone, and in stimulating angiogenesis to bring blood to hypoxic tissue. We are also interested in how mitochondrial reactive oxygen species and protein arginine methylation regulate these important beneficial effects of endothelial cell calcium signaling. We therefore are also interested in the differences between homeostatic and pathological calcium signaling, and where the inflection points between the two exist.

Lab Members:
Sarah Abdullah – graduate student

Endothelial Cell Biology

Vascular Physiology

Protein Arginine Methylation

Ca2+ Signaling