Literature DB >> 22805778

Characteristics of aquaporin expression surrounding senile plaques and cerebral amyloid angiopathy in Alzheimer disease.

Akihiko Hoshi1, Teiji Yamamoto, Keiko Shimizu, Yoshikazu Ugawa, Masatoyo Nishizawa, Hitoshi Takahashi, Akiyoshi Kakita.   

Abstract

Senile plaques (SPs) containing amyloid β peptide (Aβ) 1-42 are the major species present in Alzheimer disease (AD), whereas Aβ1-40 is the major constituent of arteriolar walls affected by cerebral amyloid angiopathy. The water channel proteins astrocytic aquaporin 1 (AQP1) and aquaporin 4 (AQP4) are known to be abnormally expressed in AD brains, but the expression of AQPs surrounding SPs and cerebral amyloid angiopathy has not been described in detail. Here, we investigated whether AQP expression is associated with each species of Aβ deposited in human brains affected by either sporadic or familial AD. Immunohistochemical analysis demonstrated more numerous AQP1-positive reactive astrocytes in the AD cerebral cortex than in controls, located close to Aβ42- or Aβ40-positive SPs. In AD cases, however, AQP1-positive astrocytes were not often observed in Aβ-rich areas, and there was a significant negative correlation between the levels of AQP1 and Aβ42 assessed semiquantitatively. We also found that Aβ plaque-like AQP4 was distributed in association with Aβ42- or Aβ40-positive SPs and that the degree of AQP4 expression around Aβ40-positive vessels was variable. These findings suggest that a defined population of AQP1-positive reactive astrocytes may modify Aβ deposition in the AD brain, whereas the Aβ deposition process might alter astrocytic expression of AQP4.

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Year:  2012        PMID: 22805778     DOI: 10.1097/NEN.0b013e3182632566

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  42 in total

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Review 3.  The Potential Roles of Aquaporin 4 in Alzheimer's Disease.

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4.  Glymphatic fluid transport controls paravascular clearance of AAV vectors from the brain.

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5.  Vascular amyloidosis impairs the gliovascular unit in a mouse model of Alzheimer's disease.

Authors:  Ian F Kimbrough; Stefanie Robel; Erik D Roberson; Harald Sontheimer
Journal:  Brain       Date:  2015-11-23       Impact factor: 13.501

Review 6.  Blood-brain barrier dysfunction as a cause and consequence of Alzheimer's disease.

Authors:  Michelle A Erickson; William A Banks
Journal:  J Cereb Blood Flow Metab       Date:  2013-08-07       Impact factor: 6.200

7.  Impairment of paravascular clearance pathways in the aging brain.

Authors:  Benjamin T Kress; Jeffrey J Iliff; Maosheng Xia; Minghuan Wang; Helen S Wei; Douglas Zeppenfeld; Lulu Xie; Hongyi Kang; Qiwu Xu; Jason A Liew; Benjamin A Plog; Fengfei Ding; Rashid Deane; Maiken Nedergaard
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Review 8.  Glymphatic System Impairment in Alzheimer's Disease and Idiopathic Normal Pressure Hydrocephalus.

Authors:  Benjamin C Reeves; Jason K Karimy; Adam J Kundishora; Humberto Mestre; H Mert Cerci; Charles Matouk; Seth L Alper; Iben Lundgaard; Maiken Nedergaard; Kristopher T Kahle
Journal:  Trends Mol Med       Date:  2020-01-18       Impact factor: 11.951

9.  Non-productive angiogenesis disassembles Aß plaque-associated blood vessels.

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Journal:  Nat Commun       Date:  2021-05-25       Impact factor: 14.919

Review 10.  Physiological and Pathological Factors Affecting Drug Delivery to the Brain by Nanoparticles.

Authors:  Yamir Islam; Andrew G Leach; Jayden Smith; Stefano Pluchino; Christopher R Coxon; Muttuswamy Sivakumaran; James Downing; Amos A Fatokun; Meritxell Teixidò; Touraj Ehtezazi
Journal:  Adv Sci (Weinh)       Date:  2021-03-15       Impact factor: 16.806

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