Granzyme-b is involved in mediating post-ischemic neuronal death during focal cerebral ischemia in rat model
Although peripheral immune cells infiltrate ischemic infarct tissue and elicit immune injury, the role of Cytotoxic T Lymphocytes (CTLs) and the toxins they release in mediating neuronal death is not well understood. Granzyme-b (Gra-b), a serine protease found in the cytoplasmic granules of CTLs and...
Gespeichert in:
| Hauptverfasser: | , , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2010
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| In: |
Neuroscience
Year: 2010, Jahrgang: 165, Heft: 4, Pages: 1203-1216 |
| ISSN: | 1873-7544 |
| DOI: | 10.1016/j.neuroscience.2009.10.067 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.neuroscience.2009.10.067
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| Verfasserangaben: | G.V. Chaitanya, M. Schwaninger, J.S. Alexander, P. Prakash Babu |
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| 245 | 1 | 0 | |a Granzyme-b is involved in mediating post-ischemic neuronal death during focal cerebral ischemia in rat model |c G.V. Chaitanya, M. Schwaninger, J.S. Alexander, P. Prakash Babu |
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| 520 | |a Although peripheral immune cells infiltrate ischemic infarct tissue and elicit immune injury, the role of Cytotoxic T Lymphocytes (CTLs) and the toxins they release in mediating neuronal death is not well understood. Granzyme-b (Gra-b), a serine protease found in the cytoplasmic granules of CTLs and natural killer cells, plays an important role in inducing target cell death by activating several caspases and by initiating caspase-independent pathways that contribute to target cell death. To determine if CTLs and Gra-b are involved in post-ischemic cerebral cell death; we investigated the role of CD8(+) CTLs and Gra-b in ischemic rat brain infarct after transient middle cerebral artery occlusion (tMCAO) and in sham-operated animals. We observed that CTLs infiltrate the ischemic infarct within 1 h of reperfusion. There was a significant increase in Gra-b levels in the ischemic region starting from 1 h until 3 day which correlated with increased levels of chemokines (IP-10/CXCL10, IL-2) and TNF-alpha. Co-immunoprecipitation experiments show that Gra-b interacts with Bid, PARP, and caspase-3 in ischemic samples. Immunofluorescence analysis of Gra-b and TUNEL showed that Gra-b is present both in apoptotic and necrotic cells. Triple immunostaining further confirmed that the Gra-b positive degenerating cells were neurons. CTLs in close spatial proximity to degenerating neurons, increased levels of Gra-b, localization in neurons positive for TUNEL, and interaction with other pro-apoptotic proteins indicate that Gra-b and CTLs play a significant role in neuronal death following cerebral ischemia in the rat brain after tMCAO. Based on the above findings we support our hypothesis that Gra-b secreted from activated CTLs might be involved in aggravating post-ischemic damage by mediating neuronal death. | ||
| 650 | 4 | |a Animals | |
| 650 | 4 | |a Apoptosis | |
| 650 | 4 | |a Brain | |
| 650 | 4 | |a Brain Ischemia | |
| 650 | 4 | |a CD8 Antigens | |
| 650 | 4 | |a Cell Death | |
| 650 | 4 | |a Disease Models, Animal | |
| 650 | 4 | |a Granzymes | |
| 650 | 4 | |a Infarction, Middle Cerebral Artery | |
| 650 | 4 | |a Male | |
| 650 | 4 | |a Necrosis | |
| 650 | 4 | |a Nerve Degeneration | |
| 650 | 4 | |a Neurons | |
| 650 | 4 | |a PC12 Cells | |
| 650 | 4 | |a Random Allocation | |
| 650 | 4 | |a Rats | |
| 650 | 4 | |a Rats, Wistar | |
| 650 | 4 | |a T-Lymphocytes, Cytotoxic | |
| 650 | 4 | |a Time Factors | |
| 700 | 1 | |a Schwaninger, Markus |e VerfasserIn |0 (DE-588)1028374909 |0 (DE-627)730623939 |0 (DE-576)375910174 |4 aut | |
| 700 | 1 | |a Alexander, J. S. |e VerfasserIn |4 aut | |
| 700 | 1 | |a Babu, P. Prakash |e VerfasserIn |4 aut | |
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