SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Kvist Ulf)
 

Sökning: WFRF:(Kvist Ulf) > Elevated MARK2-Depe...

Elevated MARK2-Dependent Phosphorylation of Tau in Alzheimer's Disease

Gu, Gucci Jijuan, 1984- (författare)
Uppsala universitet,Molekylära verktyg,Science for Life Laboratory, SciLifeLab,Prof. Ulf Landegren
Wu, Di (författare)
Uppsala universitet,Molekylära verktyg,Science for Life Laboratory, SciLifeLab,Prof. Ulf Landegren
Lund, Harald (författare)
Karolinska Institutet
visa fler...
Sunnemark, Dan (författare)
Dept. of Neuroscience, iMed, CNS and Pain Södertälje, AstraZeneca Research and Development
Kvist, Alexander (författare)
Antibody Generation Group, Discovery Sciences, iMed, AstraZeneca Research and Development
Milner, Roy (författare)
Antibody Generation Group, Discovery Sciences, iMed, AstraZeneca Research and Development
Eckersley, Sonia (författare)
Antibody Generation Group, Discovery Sciences, iMed, AstraZeneca Research and Development
Nilsson, Lars (författare)
Uppsala universitet,Geriatrik
Agerman, Karin (författare)
Dept. of Neuroscience, iMed, CNS and Pain Södertälje, AstraZeneca Research and Development
Landegren, Ulf (författare)
Uppsala universitet,Molekylära verktyg,Science for Life Laboratory, SciLifeLab
Kamali‐Moghaddam, Masood (författare)
Uppsala universitet,Institutionen för immunologi, genetik och patologi,Science for Life Laboratory, SciLifeLab
visa färre...
 (creator_code:org_t)
2013
2013
Engelska.
Ingår i: Journal of Alzheimer's Disease. - 1387-2877 .- 1875-8908. ; 33:3, s. 699-713
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The appearance of neurofibrillary tangles (NFT), one of the major hallmarks of Alzheimer's disease (AD), is most likely caused by inappropriate phosphorylation and/or dephosphorylation of tau, eventually leading to the accumulation of NFTs. Enhanced phosphorylation of tau on Ser(262) is detected early in the course of the disease and may have a role in the formation of tangles. Several kinases such as microtubule-affinity regulating kinase (MARK), protein kinase A, calcium calmodulin kinase II, and checkpoint kinase 2 are known to phosphorylate tau on Ser(262) in vitro. In this study, we took advantage of the in situ proximity ligation assay to investigate the role of MARK2, one of the four MARK isoforms, in AD. We demonstrate that MARK2 interacts with tau and phosphorylates tau at Ser(262) in stably transfected NIH/3T3 cells expressing human recombinant tau. Staurosporine, a protein kinase inhibitor, significantly reduced the interaction between MARK2 and tau, and also phosphorylation of tau at Ser(262). Furthermore, we observed elevated interactions between MARK2 and tau in post-mortem human AD brains, compared to samples from non-demented elderly controls. Our results from transfected cells demonstrate a specific interaction between MARK2 and tau, as well as MARK2-dependent phosphorylation of tau at Ser(262). Furthermore, the elevated interactions between MARK2 and tau in AD brain sections suggests that MARK2 may play an important role in early phosphorylation of tau in AD, possibly qualifying as a therapeutic target for intervention to prevent disease progression.

Ämnesord

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

Alzheimer's disease
MARK
phosphorylation
proximity ligation assay
tau

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)
kfu (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy