Neuroimmune Support of Neuronal Regeneration and Neuroplasticity following Cerebral Ischemia in Juvenile Mice.

cerebral ischemia functional recovery neural regeneration neurogenesis neuroimmune signaling synaptic plasticity

Journal

Brain sciences
ISSN: 2076-3425
Titre abrégé: Brain Sci
Pays: Switzerland
ID NLM: 101598646

Informations de publication

Date de publication:
17 Sep 2023
Historique:
received: 19 08 2023
revised: 13 09 2023
accepted: 15 09 2023
medline: 28 9 2023
pubmed: 28 9 2023
entrez: 28 9 2023
Statut: epublish

Résumé

Ischemic damage to the brain and loss of neurons contribute to functional disabilities in many stroke survivors. Recovery of neuroplasticity is critical to restoration of function and improved quality of life. Stroke and neurological deficits occur in both adults and children, and yet it is well documented that the developing brain has remarkable plasticity which promotes increased post-ischemic functional recovery compared with adults. However, the mechanisms underlying post-stroke recovery in the young brain have not been fully explored. We observed opposing responses to experimental cerebral ischemia in juvenile and adult mice, with substantial neural regeneration and enhanced neuroplasticity detected in the juvenile brain that was not found in adults. We demonstrate strikingly different stroke-induced neuroimmune responses that are deleterious in adults and protective in juveniles, supporting neural regeneration and plasticity. Understanding age-related differences in neuronal repair and regeneration, restoration of neural network function, and neuroimmune signaling in the stroke-injured brain may offer new insights for the development of novel therapeutic strategies for stroke rehabilitation.

Identifiants

pubmed: 37759938
pii: brainsci13091337
doi: 10.3390/brainsci13091337
pmc: PMC10526826
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM134974
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS131484
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20GM134974
Pays : United States
Organisme : NINDS NIH HHS
ID : R01NS131484
Pays : United States

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Auteurs

Ricaurte A Marquez-Ortiz (RA)

Department of Cellular Biology and Anatomy, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Vesna Tesic (V)

Department of Neurology, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Daniel R Hernandez (DR)

Department of Cellular Biology and Anatomy, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Bilkis Akhter (B)

Department of Cellular Biology and Anatomy, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Nibedita Aich (N)

Department of Cellular Biology and Anatomy, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Porter M Boudreaux (PM)

Department of Cellular Biology and Anatomy, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Garrett A Clemons (GA)

Department of Cellular Biology and Anatomy, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Celeste Yin-Chieh Wu (CY)

Department of Neurology, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Hung Wen Lin (HW)

Department of Cellular Biology and Anatomy, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.
Department of Neurology, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.
Department of Pharmacology, Toxicology, and Neuroscience, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Krista M Rodgers (KM)

Department of Cellular Biology and Anatomy, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.
Department of Neurology, Louisiana State University, Health Sciences Center, Shreveport, LA 70803, USA.

Classifications MeSH