Anne Kasus-Jacobi, Ph.D.
My lab currently focuses on two research projects that aim at uncovering the molecular mechanisms by which the cationic antimicrobial protein CAP37 is affecting (1) corneal wound healing and (2) neuroinflammation, with the long-term goal of developing peptide therapeutics for ocular injuries and Alzheimer’s disease.
In collaboration with Dr. Pereira, we found that the antimicrobial and inflammatory mediator CAP37, and several CAP37-derived antimicrobial peptides could promote corneal wound healing andclearance of corneal infections in vivo. Recently, my lab started to focus on the identification of the molecular mechanisms involved in the wound healing activity of CAP37 and CAP37-derived peptides. The goal of this project is the identification of the receptor and intracellular signaling molecules mediating CAP37-induced corneal wound healing.
In collaboration with Dr. Pereira, we also explored the potential roles of CAP37 in diseases linked to aging and chronic inflammation. We have shown increased expression of CAP37 in the neurons of patients with Alzheimer’s disease, and an effect of CAP37 on two important players of this disease; amyloid beta and the Receptor for Advanced Glycation End-products (RAGE). To pursue this line of research, my lab is currently exploring the structural aspects of CAP37’s effects on RAGE and amyloid beta. This project, funded by the Oklahoma COBRE in Structural Biology, was started in 2017.
Publications & Presentations
- 1. Kasus-Jacobi A, Washburn J, Land C, Pereira A. Neutrophil Granule Proteins Inhibit Amyloid Beta Aggregation and Neurotoxicity. Current Alzheimer Research. 2021; 18 : 414-427
2. Kasus-Jacobi A, Land C, Stock A, Washburn J, Pereira A. Antimicrobial peptides derived from the immune defense protein CAP37 inhibit TLR4 activation by S100A9. Investigative Ophthalmology & Visual Science/Association for Research in Vision and Ophthalmology. 2020
3. Stock A J, Kasus-Jacobi A, Pereira A. The role of neutrophil granule proteins in neuroinflammation and Alzheimer's disease. Journal of neuroinflammation. 2018; 15 : 240
4. Kasus-Jacobi A, Griffith G L, Lerner M, Pereira A. Effect of Cationic Antimicrobial Protein CAP37 on Cytokine Profile during Corneal Wound Healing. Journal of Ocular Diseases and Therapeutics. 2017; 5 : 19-27
5. Griffith G L, Kasus-Jacobi A, Pereira A. Bioactive Antimicrobial Peptides as Therapeutics for Corneal Wounds and Infections. Advances in wound care. 2017; 6 : 175-190
- 1. Novel Ophthalmic Product for Corneal Infections and Injuries. NIH. Start Date: 2021. End Date: 2022.
2. The Midwest Biomedical Accelerator Consortium (MBArC)/ Subaward - Multi-Target Peptide: A Drug to Remember. NIH. Start Date: 2021. End Date: 2022.
3. OU Growth Fund- Multi-Target Peptide: A Drug to Remember. Misc Non-Federal. Start Date: 2021. End Date: 2022.
4. Peptide Therapeutics for Treating Alzheimer’s Disease. NIH. Start Date: 2020. End Date: 2021.
5. Ocular Product Development. Non-federal. Start Date: 2020. End Date: 2021.
Awards and Honors
- 6. OUHSC/Office of Technology Development. Growth Fund Phase 1, Market Discovery. Date: 2019.
7. PHF. PHF Bridge Grant. Date: 2019.
8. NIH/NIGMS. Oklahoma COBRE in Structural Biology . Date: 2017.
9. NIH/NEI. NIH Exploratory/Developmental Research Grant Award (R21). Date: 2016.
10. NIH/NIGMS. Oklahoma Shared Clinical and Translational Resources (OSCTR) Pilot Project Grant. Date: 2016.
- 1. Degree: Ph D. University of Paris XI. Date: 1998.
2. Degree: MS. University of Paris VII. Date: 1993.
3. Degree: BS. University of Paris VII. Date: 1992.