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We are analyzing https://link.springer.com/article/10.1007/s12264-022-00847-4.

Title:
Multiple Mild Stimulations Reduce Membrane Distribution of CX3CR1 Promoted by Annexin a1 in Microglia to Attenuate Excessive Dendritic Spine Pruning and Cognitive Deficits Caused by a Transient Ischemic Attack in Mice | Neuroscience Bulletin
Description:
A transient ischemic attack (TIA) can cause reversible and delayed impairment of cognition, but the specific mechanisms are still unclear. Annexin a1 (ANXA1) is a phospholipid-binding protein. Here, we confirmed that cognition and hippocampal synapses were impaired in TIA-treated mice, and this could be rescued by multiple mild stimulations (MMS). TIA promoted the interaction of ANXA1 and CX3CR1, increased the membrane distribution of CX3CR1 in microglia, and thus enhanced the CX3CR1 and CX3CL1 interaction. These phenomena induced by TIA could be reversed by MMS. Meanwhile, the CX3CR1 membrane distribution and CX3CR1โ€“CX3CL1 interaction were upregulated in primary cultured microglia overexpressing ANXA1, and the spine density was significantly reduced in co-cultured microglia overexpressing ANXA1 and neurons. Moreover, ANXA1 overexpression in microglia abolished the protection of MMS after TIA. Collectively, our study provides a potential strategy for treating the delayed synaptic injury caused by TIA.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Education
  • Science
  • Telecommunications

Content Management System {๐Ÿ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {๐Ÿ“ˆ}

What is the average monthly size of link.springer.com audience?

๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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Keywords {๐Ÿ”}

article, google, scholar, cas, microglia, stroke, ischemic, transient, wang, cxcr, neurons, annexin, attack, sun, neurosci, china, brain, council, nat, spine, pruning, zheng, shao, zhou, shi, access, science, privacy, cookies, content, multiple, mild, membrane, xing, ning, jing, tia, anxa, synaptic, microglial, information, publish, research, search, stimulations, distribution, dendritic, cognitive, huijuan, interaction,

Topics {โœ’๏ธ}

multiple mild stimulations month download article/chapter aml1/eto aml cells ning sunย &ย jing shi a1/a2 reactive astrocytes schizophrenia patient-derived models transferring mir-23a-3p cxcr7/pi3k/akt pathway stroke-related prognostic factors coordinated spine pruning combining multiple approaches cx3cr1 membrane distribution transient ischemic attack author information authors neuronally derived fractalkine transient ischaemic attack transient ischemic attacks annexin a1 translocates peripheral vascular disease microglial cx3cr1 impairs inter-spine competition check access instant access activated mast cells related subjects full article pdf privacy choices/manage cookies membrane distribution brain research acute ischemic stroke depression-related behaviour cx3cr1-expressing microglia dendritic organization normal brain development xing li transient forebrain ischemia ncm-treated microglia annexin a1 cognitive deficits caused microglia remodel synapses european economic area phospholipid-binding protein late-onset epileptogenesis dynamic cellular mediators forming somatic junctions murine postcapillary venules linking ca2+ signalling delayed neuronal death morris water maze modulating ikkฮฑ stability

Questions {โ“}

  • Effects of environmental enrichment and voluntary exercise on neurogenesis, learning and memory, and pattern separation: BDNF as a critical variable?

Schema {๐Ÿ—บ๏ธ}

WebPage:
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         headline:Multiple Mild Stimulations Reduce Membrane Distribution of CX3CR1 Promoted by Annexin a1 in Microglia to Attenuate Excessive Dendritic Spine Pruning and Cognitive Deficits Caused by a Transient Ischemic Attack in Mice
         description:A transient ischemic attack (TIA) can cause reversible and delayed impairment of cognition, but the specific mechanisms are still unclear. Annexin a1 (ANXA1) is a phospholipid-binding protein. Here, we confirmed that cognition and hippocampal synapses were impaired in TIA-treated mice, and this could be rescued by multiple mild stimulations (MMS). TIA promoted the interaction of ANXA1 and CX3CR1, increased the membrane distribution of CX3CR1 in microglia, and thus enhanced the CX3CR1 and CX3CL1 interaction. These phenomena induced by TIA could be reversed by MMS. Meanwhile, the CX3CR1 membrane distribution and CX3CR1โ€“CX3CL1 interaction were upregulated in primary cultured microglia overexpressing ANXA1, and the spine density was significantly reduced in co-cultured microglia overexpressing ANXA1 and neurons. Moreover, ANXA1 overexpression in microglia abolished the protection of MMS after TIA. Collectively, our study provides a potential strategy for treating the delayed synaptic injury caused by TIA.
         datePublished:2022-03-30T00:00:00Z
         dateModified:2022-03-30T00:00:00Z
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            CX3CR1
            Microglia
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            Anesthesiology
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            Pain Medicine
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               1995-8218
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      headline:Multiple Mild Stimulations Reduce Membrane Distribution of CX3CR1 Promoted by Annexin a1 in Microglia to Attenuate Excessive Dendritic Spine Pruning and Cognitive Deficits Caused by a Transient Ischemic Attack in Mice
      description:A transient ischemic attack (TIA) can cause reversible and delayed impairment of cognition, but the specific mechanisms are still unclear. Annexin a1 (ANXA1) is a phospholipid-binding protein. Here, we confirmed that cognition and hippocampal synapses were impaired in TIA-treated mice, and this could be rescued by multiple mild stimulations (MMS). TIA promoted the interaction of ANXA1 and CX3CR1, increased the membrane distribution of CX3CR1 in microglia, and thus enhanced the CX3CR1 and CX3CL1 interaction. These phenomena induced by TIA could be reversed by MMS. Meanwhile, the CX3CR1 membrane distribution and CX3CR1โ€“CX3CL1 interaction were upregulated in primary cultured microglia overexpressing ANXA1, and the spine density was significantly reduced in co-cultured microglia overexpressing ANXA1 and neurons. Moreover, ANXA1 overexpression in microglia abolished the protection of MMS after TIA. Collectively, our study provides a potential strategy for treating the delayed synaptic injury caused by TIA.
      datePublished:2022-03-30T00:00:00Z
      dateModified:2022-03-30T00:00:00Z
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         Dendritic spine pruning
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         Neurosciences
         Human Physiology
         Anesthesiology
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         Neurology
         Pain Medicine
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            1995-8218
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         name:Springer Nature Singapore
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            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
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      author:
            name:Lu Zheng
            affiliation:
                  name:Tongji Medical College, Huazhong University of Science and Technology
                  address:
                     name:Department of Neurobiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
                     type:PostalAddress
                  type:Organization
                  name:Key Laboratory of Neurological Diseases, Ministry of Education
                  address:
                     name:Key Laboratory of Neurological Diseases, Ministry of Education, Wuhan, China
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                  name:Huazhong University of Science and Technology
                  address:
                     name:The Institute for Brain Research, Collaborative Innovation Center for Brain Science, Huazhong University of Science and Technology, Wuhan, China
                     type:PostalAddress
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            name:Yi Wang
            affiliation:
                  name:Tongji Medical College, Huazhong University of Science and Technology
                  address:
                     name:Department of Neurobiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
                     type:PostalAddress
                  type:Organization
                  name:Key Laboratory of Neurological Diseases, Ministry of Education
                  address:
                     name:Key Laboratory of Neurological Diseases, Ministry of Education, Wuhan, China
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                  name:Huazhong University of Science and Technology
                  address:
                     name:The Institute for Brain Research, Collaborative Innovation Center for Brain Science, Huazhong University of Science and Technology, Wuhan, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Bin Shao
            affiliation:
                  name:Tongji Medical College, Huazhong University of Science and Technology
                  address:
                     name:Department of Neurobiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
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                     name:Key Laboratory of Neurological Diseases, Ministry of Education, Wuhan, China
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                  address:
                     name:The Institute for Brain Research, Collaborative Innovation Center for Brain Science, Huazhong University of Science and Technology, Wuhan, China
                     type:PostalAddress
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            type:Person
            name:Huijuan Zhou
            affiliation:
                  name:Tongji Medical College, Huazhong University of Science and Technology
                  address:
                     name:Department of Neurobiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
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                  type:Organization
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                  name:Tongji Medical College, Huazhong University of Science and Technology
                  address:
                     name:Department of Neurobiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
                     type:PostalAddress
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                     name:Key Laboratory of Neurological Diseases, Ministry of Education, Wuhan, China
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                  address:
                     name:The Institute for Brain Research, Collaborative Innovation Center for Brain Science, Huazhong University of Science and Technology, Wuhan, China
                     type:PostalAddress
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