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Verfasst von:Mracskó, Eva [VerfasserIn]   i
 Kahn-Ziech, Alexandra Paula [VerfasserIn]   i
 Veltkamp, Roland [VerfasserIn]   i
Titel:Leukocyte invasion of the brain after experimental intracerebral hemorrhage in mice
Verf.angabe:Eva Mracsko, Ehsan Javidi, Shin-Young Na, Alexandra Kahn, Arthur Liesz, and Roland Veltkamp
E-Jahr:2014
Jahr:10 Jun 2014
Umfang:8 S.
Fussnoten:Gesehen am 23.09.2020
Titel Quelle:Enthalten in: Stroke
Ort Quelle:New York, NY : Association, 1970
Jahr Quelle:2014
Band/Heft Quelle:45(2014), 7, Seite 2107-2114
ISSN Quelle:1524-4628
Abstract:Background and Purpose: Neuroinflammatory processes contribute to secondary neuronal damage after intracerebral hemorrhage. We aimed to characterize the time course of brain immigration of different leukocyte subsets after striatal injection of either autologous blood or collagenase in mice. Methods: Intracerebral hemorrhage was induced by injection of either autologous blood (20 μL) or collagenase (0.03 U) in C57Bl/6J mice. Hematoma volumetry was performed on cryosections. Blood volume was measured by hemoglobin spectrophotometry. Leukocytes were isolated from hemorrhagic hemisphere 1, 3, 5, and 14 days after intracerebral hemorrhage, stained for leukocyte markers, and measured by flow cytometry. Heterologous blood injection from CD45.1 mice was used to investigate the origin of brain-invading leukocytes. Results: Collagenase injection induced a larger hematoma volume but a similar blood content compared with blood injection. Cerebral leukocyte infiltration in the hemorrhagic hemisphere was similar in both models. The majority of leukocytes isolated from the brain originated from the circulation. CD4+ T lymphocytes were the predominant brain leukocyte population in both models. However, cerebral granulocyte counts were higher after collagenase compared with blood injection. Conclusions: Brain infiltration of systemic immune cells is similar in both murine intracerebral hemorrhage models. The pathophysiological impact of invading leukocytes and, in particular, of T cells requires further investigation.
DOI:doi:10.1161/STROKEAHA.114.005801
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1161/STROKEAHA.114.005801
 Volltext: https://www.ahajournals.org/doi/10.1161/STROKEAHA.114.005801
 DOI: https://doi.org/10.1161/STROKEAHA.114.005801
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1733587667
Verknüpfungen:→ Zeitschrift

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