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Characterization of cell proliferation in the adult dentate under normal conditions and after kainate induced seizures using ribonucleotide reductase and BrdU.

Zhu, Hong, 1962 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för anatomi och cellbiologi,Institute of Anatomy and Cell Biology
Dahlström, Annica, 1941 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för anatomi och cellbiologi,Institute of Anatomy and Cell Biology
Hansson, Hans-Arne, 1939 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för anatomi och cellbiologi,Institute of Anatomy and Cell Biology
 (creator_code:org_t)
Elsevier BV, 2005
2005
Engelska.
Ingår i: Brain research. - : Elsevier BV. - 0006-8993. ; 1036:1-2, s. 7-17
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Ribonucleotide reductase (RNR), an enzyme for DNA synthesis, was recently used as a marker of proliferating cells in the dentate gyrus and subventricular zone in normal adult mammalian brains. However, the duration of RNR expression in normal adult brain and the expression pattern of RNR in the adult dentate gyrus following brain injury have not been explored. In this study, we examined the duration of the RNR expression in newborn cells in the normal adult rat brain by analysis of RNR and BrdU double-labeled specimens at different time intervals after BrdU application. Secondly, we induced, in adult rats, seizures by kainic acid and investigated the changes in expression of RNR following seizures, and characterized the phenotype of RNR-positive cells using a variety of other markers. Our results revealed that RNR was detectable in proliferating cells from 2 h to at least 1 day. At 7 and 28 days after seizures, there was a fivefold increase in number of clusters of RNR-positive cells in the dentate gyrus, and a doubling of the number of BrdU-labeled cells in each cluster. Proliferating astrocytes and neuronal precursors were recognized in each RNR-positive cell cluster, and both types increased in number after seizures. Colocalization of RNR and activated caspase-3 was observed at 7 days, indicating that proliferating cells were susceptible to status epilepticus induced damage. RNR immunohistochemistry provides a useful approach in experiments investigating a change in cell proliferation, revealing the location, number, morphology and fate of newly formed cells after, e.g., brain injury.

Nyckelord

Animals
Astrocytes
cytology
metabolism
Biological Markers
Bromodeoxyuridine
Caspase 3
Caspases
metabolism
Cell Death
physiology
Cell Proliferation
Convulsants
Dentate Gyrus
cytology
metabolism
Epilepsy
chemically induced
metabolism
physiopathology
Fluorescent Antibody Technique
Kainic Acid
Male
Nerve Degeneration
metabolism
physiopathology
Nerve Regeneration
physiology
Neuronal Plasticity
physiology
Neurons
cytology
metabolism
Rats
Rats
Sprague-Dawley
Recovery of Function
physiology
Ribonucleotide Reductases
metabolism
Stem Cells
cytology
metabolism
Up-Regulation
physiology

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