Literature DB >> 26811151

Effects of Aging on Neural Stem/Progenitor Cells and Oligodendrocyte Precursor Cells After Focal Cerebral Ischemia in Spontaneously Hypertensive Rats.

Anna C Liang1, Emiri T Mandeville, Takakuni Maki, Akihiro Shindo, Angel T Som, Naohiro Egawa, Kanako Itoh, Tsu Tshen Chuang, John D McNeish, Julie C Holder, Josephine Lok, Eng H Lo, Ken Arai.   

Abstract

Aging and vascular comorbidities such as hypertension comprise critical cofactors that influence how the brain responds to stroke. Ischemic stress induces neurogenesis and oligodendrogenesis in younger brains. However, it remains unclear whether these compensatory mechanisms can be maintained even under pathologically hypertensive and aged states. To clarify the age-related remodeling capacity after stroke under hypertensive conditions, we assessed infarct volume, behavioral outcomes, and surrogate markers of neurogenesis and oligodendrogenesis in acute and subacute phases after transient focal cerebral ischemia in 3- and 12-month-old spontaneously hypertensive rats (SHRs). Hematoxylin and eosin staining showed that 3- and 12-month-old SHRs exhibited similar infarction volumes at both 3 and 14 days after focal cerebral ischemia. However, recovery of behavioral deficits (neurological score assessment and adhesive removal test) was significantly less in 12-month-old SHRs compared to 3-month-old SHRs. Concomitantly, numbers of nestin(+) neural stem/progenitor cells (NSPCs) near the infarct border area or subventricular zone in 12-month-old SHRs were lower than 3-month-old SHRs at day 3. Similarly, numbers of PDGFR-α(+) oligodendrocyte precursor cells (OPCs) in the corpus callosum were lower in 12-month-old SHRs at day 3. Lower levels of NSPC and OPC numbers were accompanied by lower expression levels of phosphorylated CREB. By day 14 postischemia, NSPC and OPC numbers in 12-month-old SHRs recovered to similar levels as in 3-month-old SHRs, but the numbers of proliferating NSPCs (Ki-67(+)nestin(+) cells) and proliferating OPCs (Ki-67(+)PDGFR-α(+) cells) remained lower in the older brains even at day 14. Taken together, these findings suggest that aging may also decrease poststroke compensatory responses for neurogenesis and oligodendrogenesis even under hypertensive conditions.

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Year:  2016        PMID: 26811151      PMCID: PMC5324972          DOI: 10.3727/096368916X690557

Source DB:  PubMed          Journal:  Cell Transplant        ISSN: 0963-6897            Impact factor:   4.064


  38 in total

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6.  PDGFR alpha-positive B cells are neural stem cells in the adult SVZ that form glioma-like growths in response to increased PDGF signaling.

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8.  Stroke-induced progenitor cell proliferation in adult spontaneously hypertensive rat brain: effect of exogenous IGF-1 and GDNF.

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9.  Differential development of vascular and cardiac hypertrophy in genetic hypertension. Relation to sympathetic function.

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Review 2.  Hemorrhagic Transformation After Tissue Plasminogen Activator Treatment in Acute Ischemic Stroke.

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Review 3.  Impact of aging and comorbidities on ischemic stroke outcomes in preclinical animal models: A translational perspective.

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4.  CREB controls cortical circuit plasticity and functional recovery after stroke.

Authors:  L Caracciolo; M Marosi; J Mazzitelli; S Latifi; Y Sano; L Galvan; R Kawaguchi; S Holley; M S Levine; G Coppola; C Portera-Cailliau; A J Silva; S T Carmichael
Journal:  Nat Commun       Date:  2018-06-08       Impact factor: 17.694

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Review 6.  The effect of age-related risk factors and comorbidities on white matter injury and repair after ischemic stroke.

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7.  Promoting Neurovascular Recovery in Aged Mice after Ischemic Stroke - Prophylactic Effect of Omega-3 Polyunsaturated Fatty Acids.

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Review 8.  Particles Containing Cells as a Strategy to Promote Remyelination in Patients With Multiple Sclerosis.

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Review 9.  Opportunities and Limitations of Vascular Risk Factor Models in Studying Plasticity-Promoting and Restorative Ischemic Stroke Therapies.

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  9 in total

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