Research groups
HCEMM-USZ Cerebral Blood Flow and Metabolism Research Group
Continuous, undisturbed blood supply to the brain is essential to optimal neural function. The brain accounts for 2% of the body mass, yet it receives 15% of the cardiac output and consumes 20% of the full body's oxygen supply. Any reduction or a very brief cessation of cerebral blood flow has, therefore, a detrimental impact on brain function. The goal of our research is to understand the cellular mechanisms of neuronal injury in acute cerebrovascular disorders.
Our ongoing research focuses on ischemic stroke. The development of effective strategies to limit the progression of secondary injury is of fundamental importance to improve the prospect of successful recovery. As a first step, it is essential to recognize distinct injurious phenomena that evolve over the subacute and chronic phases of ischemic brain injury (e.g. brain edema, vasospasm, oxidative stress, excitotoxicity). The phenomenon known as spreading depolarization is a central mechanism of secondary ischemic brain injury. We explore the signaling pathways set in motion by spreading depolarizations. We also study the impact of aging on the progression of ischemic brain injury. This is a timely and pertinent area of research since the incidence of ischemic stroke increases exponentially after the age of 50 years. Our work is essentially translational; the data generated is expected to be turned into the design of effective therapies to alleviate stroke symptoms.
Members:
- Prof. Dr. Eszter Farkas
- Dr. Ákos Menyhárt
- Dr. Szilvia V. Kecskés
- Dr. Rita Frank
- Anna Törteli
- Dr. Armand Rafael Bálint
- István Pesti
- Petra Somogyi
Neuroinflammation Research Group
Different activated and ramified microglia populations in embryonic- or newborn derived primary cortical cultures can be separated with different morphological, molecular, immuncytochemical and functional (proliferation and phagocytosis capacity) methods. In our study, we explore the action of anti- and proinflammatory compounds on the re-arrangement of cytoskeletal actin in microglial cells.
We apply in our in vitro system morphological and functional assays (cell proliferation and viability, phagocytosis, motility test and several gene expression measurement-based methods). Beside the examination of transcriptional and epigenetic regulation of the pro-and anti-inflammatory gene expression, we also analyze specific intracellular signalization pathways potentially implicated in the activation of the microglia.
We manipulate environmental factors in the cultures (temperature, inflammatory and osmotic factors) in combination with the application of inhibitors of actin cell cortex re-arrangement, or modulators of inflammatory process.
Our in vitro experiments are used to replicate various aspects of neuroinflammation, neurodegeneration and regeneration (typical of Alzheimer’s or Huntington disease) and are expected to contribute to the better understanding of pro- and anti-inflammatory signaling in microglia. Our work contributes to a multidisciplinary research panel, in which the dysfunction of cellular signaling in the nervous tissue is studied to aid the development of effective therapeutic strategies for the treatment of neurodegenerative disorders.
Members