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Spontaneous astrocytic Ca 2+ activity abounds in electrically suppressed ischemic penumbra of aged mice
Experimental focal cortical ischemic lesions consist of an ischemic core and a potentially salvageable peri-ischemic region, the ischemic penumbra. The activity of neurons and astrocytes is assumed to be suppressed in the penumbra because the electrical function is interrupted, but this is incomplet...
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Published in: | Glia 2019-01, Vol.67 (1), p.37-52 |
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creator | Fordsmann, Jonas Christoffer Murmu, Reena Prity Cai, Changsi Brazhe, Alexey Thomsen, Kirsten Joan Zambach, Stefan Andreas Lønstrup, Micael Lind, Barbara Lykke Lauritzen, Martin |
description | Experimental focal cortical ischemic lesions consist of an ischemic core and a potentially salvageable peri-ischemic region, the ischemic penumbra. The activity of neurons and astrocytes is assumed to be suppressed in the penumbra because the electrical function is interrupted, but this is incompletely elucidated. Most experimental stroke studies used young adult animals, whereas stroke is prevalent in the elderly population. Using two-photon imaging in vivo, we here demonstrate extensive but electrically silent, spontaneous Ca
activity in neurons and astrocytes in the ischemic penumbra of 18- to 24-month-old mice 2-4 hr after middle cerebral artery occlusion. In comparison, stroke reduced spontaneous Ca
activity in neurons and astrocytes in adult mice (3-4 months of age). In aged mice, stroke increased astrocytic spontaneous Ca
activity considerably while neuronal spontaneous Ca
activity was unchanged. Blockade of action potentials and of purinergic receptors strongly reduced spontaneous Ca
activity in both neurons and astrocytes in the penumbra of old stroke mice. This indicates that stroke had a direct influence on mechanisms in presynaptic terminals and on purinergic signaling. Thus, highly dynamic variations in spontaneous Ca
activity characterize the electrically compromised penumbra, with remarkable differences between adult and old mice. The data are consistent with the notion that aged neurons and astrocytes take on a different phenotype than young mice. The increased activity of the aged astrocyte phenotype may be harmful to neurons. We suggest that the abundant spontaneous Ca
activity in astrocytes in the ischemic penumbra of old mice may be a novel target for neuroprotection strategies. A video abstract of this article can be found at https://youtu.be/AKlwKFsz1qE. |
doi_str_mv | 10.1002/glia.23506 |
format | article |
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activity in neurons and astrocytes in the ischemic penumbra of 18- to 24-month-old mice 2-4 hr after middle cerebral artery occlusion. In comparison, stroke reduced spontaneous Ca
activity in neurons and astrocytes in adult mice (3-4 months of age). In aged mice, stroke increased astrocytic spontaneous Ca
activity considerably while neuronal spontaneous Ca
activity was unchanged. Blockade of action potentials and of purinergic receptors strongly reduced spontaneous Ca
activity in both neurons and astrocytes in the penumbra of old stroke mice. This indicates that stroke had a direct influence on mechanisms in presynaptic terminals and on purinergic signaling. Thus, highly dynamic variations in spontaneous Ca
activity characterize the electrically compromised penumbra, with remarkable differences between adult and old mice. The data are consistent with the notion that aged neurons and astrocytes take on a different phenotype than young mice. The increased activity of the aged astrocyte phenotype may be harmful to neurons. We suggest that the abundant spontaneous Ca
activity in astrocytes in the ischemic penumbra of old mice may be a novel target for neuroprotection strategies. A video abstract of this article can be found at https://youtu.be/AKlwKFsz1qE.</description><identifier>ISSN: 0894-1491</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/glia.23506</identifier><identifier>PMID: 30427548</identifier><language>eng</language><publisher>United States</publisher><ispartof>Glia, 2019-01, Vol.67 (1), p.37-52</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c998-9d3bf486813ded46ae11192d931b602a52908772bdfb9a011420e9135ea12a43</citedby><cites>FETCH-LOGICAL-c998-9d3bf486813ded46ae11192d931b602a52908772bdfb9a011420e9135ea12a43</cites><orcidid>0000-0002-1495-4652 ; 0000-0002-7001-610X ; 0000-0002-1517-1131 ; 0000-0003-4302-7978 ; 0000-0003-3897-6474 ; 0000-0003-0027-5226 ; 0000-0002-6027-1502 ; 0000-0002-2828-7352</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30427548$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fordsmann, Jonas Christoffer</creatorcontrib><creatorcontrib>Murmu, Reena Prity</creatorcontrib><creatorcontrib>Cai, Changsi</creatorcontrib><creatorcontrib>Brazhe, Alexey</creatorcontrib><creatorcontrib>Thomsen, Kirsten Joan</creatorcontrib><creatorcontrib>Zambach, Stefan Andreas</creatorcontrib><creatorcontrib>Lønstrup, Micael</creatorcontrib><creatorcontrib>Lind, Barbara Lykke</creatorcontrib><creatorcontrib>Lauritzen, Martin</creatorcontrib><title>Spontaneous astrocytic Ca 2+ activity abounds in electrically suppressed ischemic penumbra of aged mice</title><title>Glia</title><addtitle>Glia</addtitle><description>Experimental focal cortical ischemic lesions consist of an ischemic core and a potentially salvageable peri-ischemic region, the ischemic penumbra. The activity of neurons and astrocytes is assumed to be suppressed in the penumbra because the electrical function is interrupted, but this is incompletely elucidated. Most experimental stroke studies used young adult animals, whereas stroke is prevalent in the elderly population. Using two-photon imaging in vivo, we here demonstrate extensive but electrically silent, spontaneous Ca
activity in neurons and astrocytes in the ischemic penumbra of 18- to 24-month-old mice 2-4 hr after middle cerebral artery occlusion. In comparison, stroke reduced spontaneous Ca
activity in neurons and astrocytes in adult mice (3-4 months of age). In aged mice, stroke increased astrocytic spontaneous Ca
activity considerably while neuronal spontaneous Ca
activity was unchanged. Blockade of action potentials and of purinergic receptors strongly reduced spontaneous Ca
activity in both neurons and astrocytes in the penumbra of old stroke mice. This indicates that stroke had a direct influence on mechanisms in presynaptic terminals and on purinergic signaling. Thus, highly dynamic variations in spontaneous Ca
activity characterize the electrically compromised penumbra, with remarkable differences between adult and old mice. The data are consistent with the notion that aged neurons and astrocytes take on a different phenotype than young mice. The increased activity of the aged astrocyte phenotype may be harmful to neurons. We suggest that the abundant spontaneous Ca
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activity in neurons and astrocytes in the ischemic penumbra of 18- to 24-month-old mice 2-4 hr after middle cerebral artery occlusion. In comparison, stroke reduced spontaneous Ca
activity in neurons and astrocytes in adult mice (3-4 months of age). In aged mice, stroke increased astrocytic spontaneous Ca
activity considerably while neuronal spontaneous Ca
activity was unchanged. Blockade of action potentials and of purinergic receptors strongly reduced spontaneous Ca
activity in both neurons and astrocytes in the penumbra of old stroke mice. This indicates that stroke had a direct influence on mechanisms in presynaptic terminals and on purinergic signaling. Thus, highly dynamic variations in spontaneous Ca
activity characterize the electrically compromised penumbra, with remarkable differences between adult and old mice. The data are consistent with the notion that aged neurons and astrocytes take on a different phenotype than young mice. The increased activity of the aged astrocyte phenotype may be harmful to neurons. We suggest that the abundant spontaneous Ca
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title | Spontaneous astrocytic Ca 2+ activity abounds in electrically suppressed ischemic penumbra of aged mice |
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