Student working on a research project.

Regulation Of Cytokine Production By Macrophages

Studies in Dr. Ignatowski’s laboratory are designed to investigate the bidirectional communication between the nervous and immune systems as it relates to the control of depressive behavior, chronic pain, and inflammation. She uses a combination of in vitro cell culture systems, in vivo electrical field stimulation of brain tissue, molecular methods, immunohistochemical and immunofluorescence staining, and behavioral models to address the question of how brain-derived tumor necrosis factor (TNF), a pro-inflammatory cytokine and neuromediator, functions as a modulator of brain-body interactions during neuropathic pain and in the mechanism of action of antidepressant drugs. Additionally, studies involve investigation of adrenergic regulation of TNF production from the peripheral macrophage, a major source of TNF during inflammation. Ongoing projects: (1) Study the effects of the neurotransmitter norepinephrine (NE) on the release of the cytokine TNF produced by macrophages, immune effector cells. NE-sensitive a2- and β2-adrenergic receptors on macrophages will be stimulated to assess regulation of TNF production during models of neuropathic pain and depression. Macrophage will be harvested from animals at the time of termination, and TNF production will be compared amongst the various animal groups. (2) Use immunohistochemical and immunofluorescence staining to determine whether there is a correlation between levels of TNF in rodents induced with diabetic neuropathy and the amount of neurogenesis (growth and development of neurons). We will also compare staining to samples taken from rats administered drugs that are known to alleviate pain behavior and improve depressive behavior in animals. The brains will be harvested and the hippocampi isolated. The brain tissue will be sectioned and specific antibodies will be used to stain for TNF and markers expressed by newly born immature neurons and newly dividing cells. (3)Assess inflammatory mediators, such as high-mobility group box chromosomal protein 1 (HMGB1) produced by macrophages and damaged neurons, from diabetic and control animals (rats/mice). We will determine whether animals receiving treatment for diabetic neuropathic pain have modified levels of inflammatory mediators.

Research Project Information

Disciplines: Neuroimmunology, Neuroscience, Immunology
Student Skill-Set Needed: Ability to work independently as well as with others, Cell culture techniques, Immunohistochemical staining, Data analysis, ability/willingness to work with rats/mice
Compensation: Academic Credit, Volunteer
Available: Fall, Spring, Summer

Contact

For further information on this opportunity, or to apply, contact:

Faculty Member: Tracey Ignatowski
Title: Research Associate Professor
Department: Pathology And Anatomical Sciences
Office: 27 Sherman Hall
Phone: 829-3102
Email: tai1@buffalo.edu