Meet Inspiring Speakers and Experts at our 3000+ Global Conference Series Events with over 1000+ Conferences, 1000+ Symposiums
and 1000+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business.

Explore and learn more about Conference Series : World's leading Event Organizer

Back

Ikeshima-Kataoka

Ikeshima-Kataoka

Keio University School of Medicine, Japan

Title: Reactive Astrocyte has a Neuroimmunological Function in injured Mouse Brain

Biography

Biography: Ikeshima-Kataoka

Abstract

In the central nervous system (CNS), some glial cells such as astrocytes and microglial cells become active to proliferate and secrete some of the inflammatory cytokines around lesion site when traumatic injury or inflammation occurred. However, it is still unclear for the functional role of those activated glial cells in the brain. To focus onto the regeneration of the CNS, we have been to analyze functional role of reactive glial cells in the brain with stab wound injury. As a brain injury model, stab wound using 27G needle was made on the mouse cerebral cortex from caudal to rostral axis. In the reactive astrocytes, one of the extracellular matrix molecule, tenascin-C (TN-C) is highly expressed, we analyzed TN-C functional role using TN-C-deficient mice (TN-C/KO) and found that TN-C is required for activation of astrocytes such as proliferating and induce secretion of some of the inflammatory cytokines in the injured brain and in the primary culture of astrocytes. Furthermore, TN-C has an important role for recovery of blood brain barrier (BBB) breakdown caused by stab wound in the brain. From these results, reactivation of astrocytes in the injured brain might have a functional role for BBB recovery in the CNS. On the other hand, since one of the water channels in the CNS aquaporin 4 (AQP4) is upregulated in activated astrocytes after the stab wound, we have analyzed AQP4 functional role in reactive astrocytes with injured brain using AQP4-deficient mice (AQP4/KO) compared to the wild type mouse (WT) brain. To label the proliferating cells, bromo-deoxy-uridine (BrdU) was used and that could be incorporated to the mice through the drinking water. Immuno-fluorescent staining analysis was performed on cardiac perfused mouse brain sections with