2015
Blood - cerebrospinal fluid barrier in rat after peripheral nerve injury
JOUKAL, Marek, Peter SOLÁR, Adéla KUKLOVÁ, Ilona KLUSÁKOVÁ, Petr DUBOVÝ et. al.Základní údaje
Originální název
Blood - cerebrospinal fluid barrier in rat after peripheral nerve injury
Název česky
Hematolikvorová bariéra laboratorního potkana po poškození periferního nervu
Autoři
Vydání
CEITEC PHD RETREAT, 2015
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
30000 3. Medical and Health Sciences
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Organizační jednotka
Lékařská fakulta
ISBN
978-80-210-7825-3
Klíčová slova česky
Hematolikvorová bariéra, poškození periferního nervu, FluoroEmerald, imunohistochemie
Klíčová slova anglicky
blood - cerebrospinal fluid berrier, peripheral nerve injury, FluoroEmerald, imunohistochemistry
Změněno: 25. 4. 2015 09:41, doc. MUDr. Marek Joukal, Ph.D.
Anotace
V originále
The unilateral chronical constriction injury (CCI) used as a neuropathic pain model causes the elevation of proinflammatory cytokines levels not only in the dorsal root ganglia (DRG) related to damaged nerve, but also in remote DRG and central nervous system structures. We purpose that one of the possible pathways for spread of neuroinflammation could be over the blood-cerebrospinal fluid barrier present in choroid plexus (CP). We used the intravenous injection of fluorescent conjugated dextrane (FluoroEmerald - FE) to clarify our hypothesis. Twelve Wistar male rats were divided to the 3 days (n=5) and 21 days (n=5) of CCI groups, two rats were naive. The FE was intravenously applied at time of CCI survival and rats were sacrificed after 18 hours of FE circulation, perfused transcardially by Zamboni´s fixative. Distribution of FE and simultaneous immunohistochemical detection for resident (ED2) and activated (ED1) macrophages, antigen presenting cells (APC; MHC-II) and microglia (OX-42) was studied in CP using coronal cryostat sections through the brain. FluoroEmerald particles were presented in cuboidal epithelial cells of CP. The activated macrophages, microglia and APC positive for FE were found in CP stroma. Epiplexal Kolmer cells immunostained for ED2 and MHC-II were loaded by FE. In addition, FE particles were also found in ventricular ependymal cells (EC). Our results suggest that composite effect of CCI and FE causes immune reaction in CP followed by diffusion of FE particles into EC.