Cargando…

Spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation

Inflammation following ischaemic stroke attracts high priority in current research, particularly using human-like models and long-term observation periods considering translational aspects. The present study aimed on the spatio-temporal course of macrophage-like cell accumulation after experimental...

Descripción completa

Detalles Bibliográficos
Autores principales: Michalski, D., Heindl, M., Kacza, J., Laignel, F., Küppers-Tiedt, L., Schneider, D., Grosche, J., Boltze, J., Löhr, M., Hobohm, C., Härtig, W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428963/
https://www.ncbi.nlm.nih.gov/pubmed/22688295
http://dx.doi.org/10.4081/ejh.2012.e14
_version_ 1782241749584838656
author Michalski, D.
Heindl, M.
Kacza, J.
Laignel, F.
Küppers-Tiedt, L.
Schneider, D.
Grosche, J.
Boltze, J.
Löhr, M.
Hobohm, C.
Härtig, W.
author_facet Michalski, D.
Heindl, M.
Kacza, J.
Laignel, F.
Küppers-Tiedt, L.
Schneider, D.
Grosche, J.
Boltze, J.
Löhr, M.
Hobohm, C.
Härtig, W.
author_sort Michalski, D.
collection PubMed
description Inflammation following ischaemic stroke attracts high priority in current research, particularly using human-like models and long-term observation periods considering translational aspects. The present study aimed on the spatio-temporal course of macrophage-like cell accumulation after experimental thromboembolic stroke and addressed microglial and astroglial reactions in the ischaemic border zone. Further, effects of tissue plasminogen activator (tPA) as currently best treatment for stroke and the potentially neuroprotective co-administration of hyperbaric oxygen (HBO) were investigated. Rats underwent middle cerebral artery occlusion and were assigned to control, tPA or tPA+HBO. Twenty-four hours, 7, 14 and 28 days were determined as observation time points. The accumulation of macrophage-like cells was semiquantitatively assessed by CD68 staining in the ischaemic area and ischaemic border zone, and linked to the clinical course. CD11b, ionized calcium binding adaptor molecule 1 (Iba), glial fibrillary acidic protein (GFAP) and Neuronal Nuclei (NeuN) were applied to reveal delayed glial and neuronal alterations. In all groups, the accumulation of macrophage-like cells increased distinctly from 24 hours to 7 days post ischaemia. tPA+HBO tended to decrease macrophage-like cell accumulation at day 14 and 28. Overall, a trend towards an association of increased accumulation and pronounced reduction of the neurological deficit was found. Concerning delayed inflammatory reactions, an activation of microglia and astrocytes with co-occurring neuronal loss was observed on day 28. Thereby, astrogliosis was found circularly in contrast to microglial activation directly in the ischaemic area. This study supports previous data on long-lasting inflammatory processes following experimental stroke, and additionally provides region-specific details on glial reactions. The tendency towards a decreasing macrophage-like cell accumulation after tPA+HBO needs to be discussed critically since neuroprotective properties were recently ascribed to long-term inflammatory processes.
format Online
Article
Text
id pubmed-3428963
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher PAGEPress Publications
record_format MEDLINE/PubMed
spelling pubmed-34289632012-08-29 Spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation Michalski, D. Heindl, M. Kacza, J. Laignel, F. Küppers-Tiedt, L. Schneider, D. Grosche, J. Boltze, J. Löhr, M. Hobohm, C. Härtig, W. Eur J Histochem Original Paper Inflammation following ischaemic stroke attracts high priority in current research, particularly using human-like models and long-term observation periods considering translational aspects. The present study aimed on the spatio-temporal course of macrophage-like cell accumulation after experimental thromboembolic stroke and addressed microglial and astroglial reactions in the ischaemic border zone. Further, effects of tissue plasminogen activator (tPA) as currently best treatment for stroke and the potentially neuroprotective co-administration of hyperbaric oxygen (HBO) were investigated. Rats underwent middle cerebral artery occlusion and were assigned to control, tPA or tPA+HBO. Twenty-four hours, 7, 14 and 28 days were determined as observation time points. The accumulation of macrophage-like cells was semiquantitatively assessed by CD68 staining in the ischaemic area and ischaemic border zone, and linked to the clinical course. CD11b, ionized calcium binding adaptor molecule 1 (Iba), glial fibrillary acidic protein (GFAP) and Neuronal Nuclei (NeuN) were applied to reveal delayed glial and neuronal alterations. In all groups, the accumulation of macrophage-like cells increased distinctly from 24 hours to 7 days post ischaemia. tPA+HBO tended to decrease macrophage-like cell accumulation at day 14 and 28. Overall, a trend towards an association of increased accumulation and pronounced reduction of the neurological deficit was found. Concerning delayed inflammatory reactions, an activation of microglia and astrocytes with co-occurring neuronal loss was observed on day 28. Thereby, astrogliosis was found circularly in contrast to microglial activation directly in the ischaemic area. This study supports previous data on long-lasting inflammatory processes following experimental stroke, and additionally provides region-specific details on glial reactions. The tendency towards a decreasing macrophage-like cell accumulation after tPA+HBO needs to be discussed critically since neuroprotective properties were recently ascribed to long-term inflammatory processes. PAGEPress Publications 2012-05-09 /pmc/articles/PMC3428963/ /pubmed/22688295 http://dx.doi.org/10.4081/ejh.2012.e14 Text en ©Copyright D. Michalski et al., 2012 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy
spellingShingle Original Paper
Michalski, D.
Heindl, M.
Kacza, J.
Laignel, F.
Küppers-Tiedt, L.
Schneider, D.
Grosche, J.
Boltze, J.
Löhr, M.
Hobohm, C.
Härtig, W.
Spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation
title Spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation
title_full Spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation
title_fullStr Spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation
title_full_unstemmed Spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation
title_short Spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation
title_sort spatio-temporal course of macrophage-like cell accumulation after experimental embolic stroke depending on treatment with tissue plasminogen activator and its combination with hyperbaric oxygenation
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428963/
https://www.ncbi.nlm.nih.gov/pubmed/22688295
http://dx.doi.org/10.4081/ejh.2012.e14
work_keys_str_mv AT michalskid spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT heindlm spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT kaczaj spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT laignelf spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT kupperstiedtl spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT schneiderd spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT groschej spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT boltzej spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT lohrm spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT hobohmc spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation
AT hartigw spatiotemporalcourseofmacrophagelikecellaccumulationafterexperimentalembolicstrokedependingontreatmentwithtissueplasminogenactivatoranditscombinationwithhyperbaricoxygenation