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Spatial Distribution of DARPP-32 in Dendritic Spines

Blom, Hans (författare)
KTH,Cellens fysik,Science for Life Laboratory, SciLifeLab
Rönnlund, Daniel (författare)
KTH,Experimentell biomolekylär fysik
Scott, L. (författare)
Karolinska Institutet
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Westin, L. (författare)
Widengren, Jerker (författare)
KTH,Experimentell biomolekylär fysik,Science for Life Laboratory, SciLifeLab
Aperia, A. (författare)
Karolinska Institutet
Brismar, Hjalmar (författare)
Karolinska Institutet,KTH,Cellens fysik,Science for Life Laboratory, SciLifeLab
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 (creator_code:org_t)
2013-09-10
2013
Engelska.
Ingår i: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 8:9, s. e75155-
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The phosphoprotein DARPP-32 (dopamine and cyclic adenosine 3́, 5́-monophosphate-regulated phosphoprotein, 32 kDa) is an important component in the molecular regulation of postsynaptic signaling in neostriatum. Despite the importance of this phosphoprotein, there is as yet little known about the nanoscale distribution of DARPP-32. In this study we applied superresolution stimulated emission depletion microscopy (STED) to assess the expression and distribution of DARPP-32 in striatal neurons. Primary culture of striatal neurons were immunofluorescently labeled for DARPP-32 with Alexa-594 and for the dopamine D1 receptor (D1R) with atto-647N. Dual-color STED microscopy revealed discrete localizations of DARPP-32 and D1R in the spine structure, with clustered distributions in both head and neck. Dissected spine structures reveal that the DARPP-32 signal rarely overlapped with the D1R signal. The D1R receptor is positioned in an "aggregated" manner primarily in the spine head and to some extent in the neck, while DARPP-32 forms several neighboring small nanoclusters spanning the whole spine structure. The DARPP-32 clusters have a mean size of 52 +/- 6 nm, which is close to the resolution limit of the microscope and corresponds to the physical size of a few individual phosphoprotein immunocomplexes. Dissection of synaptic proteins using superresolution microscopy gives possibilities to reveal in better detail biologically relevant information, as compared to diffraction-limited microscopy. In this work, the dissected postsynaptic topology of the DARPP-32 phosphoprotein provides strong evidence for a compartmentalized and confined distribution in dendritic spines. The protein topology and the relatively low copy number of phosphoprotein provides a conception of DARPP-32's possibilities to fine-tune the regulation of synaptic signaling, which should have an impact on the performance of the neuronal circuits in which it is expressed.

Ämnesord

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Nyckelord

dopamine 1 receptor
phosphoprotein DARPP 32
animal cell
article
cell aggregation
cellular distribution
corpus striatum
dendritic spine
embryo
microscopy
nonhuman
protein expression
protein localization
rat
signal transduction
stimulated emission depletion microscopy

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