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Maria Thereza Perez

Senior Lecturer

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Mitogen-activated protein kinases in the porcine retinal arteries and neuroretina following retinal ischemia-reperfusion.

Author

  • Bodil Gesslein
  • Gisela Håkansson
  • Ronald Carpio
  • Lotta Gustafsson
  • Maria Thereza Perez
  • Malin Malmsjö

Summary, in English

PURPOSE: The aim of the present study was to examine changes in the expression of intracellular signal-transduction pathways, specifically mitogen-activated protein kinases, following retinal ischemia-reperfusion. METHODS: Retinal ischemia was induced by elevating the intraocular pressure in porcine eyes, followed by 5, 12, or 20 h of reperfusion. The results were compared to those of the sham- operated fellow eye. The retinal arteries and neuroretina were isolated separately and examined. Tissue morphology and DNA fragmentation were studied using histology. Extracellular signal-regulated kinase 1 and 2 (ERK1/2), p38, c-junNH(2)-terminal kinases (JNK), and c-jun protein and mRNA expression were examined using immunofluorescence staining, western blot, and real-time PCR techniques. RESULTS: Pyknotic cell nuclei, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL)-positive cells, and glial fibrillary acidic protein mRNA expression were increased in ischemia, suggesting injury. Phosphorylated ERK1/2 protein levels were increased in the neuroretina following ischemia, while mRNA levels were unaltered. p38 protein and mRNA levels were not affected by ischemia. Immunofluorescence staining for phosphorylated p38 was especially intense in the retinal blood vessels, while only weak in the neuroretina. Phosphorylated JNK protein and mRNA were slightly decreased in ischemia. Phosphorylated c-jun protein and mRNA levels were higher in the neuroretina after ischemia-reperfusion. CONCLUSIONS: Retinal ischemia-reperfusion alters expression of mitogen-activated protein kinases, particularly ERK1/2, in the neuroretina and retinal arteries. The development of pharmacological treatment targeting these intracellular transduction pathways may prevent injury to the eye following retinal circulatory failure.

Department/s

  • Medicine, Lund
  • Ophthalmology, Lund
  • Clinical Chemistry, Malmö
  • Nanomaterials for retinal prostheses

Publishing year

2010

Language

English

Pages

392-407

Publication/Series

Molecular Vision

Volume

16

Document type

Journal article

Publisher

Molecular Vision

Topic

  • Biochemistry and Molecular Biology

Status

Published

Research group

  • Clinical Chemistry, Malmö
  • Nanomaterials for retinal prostheses

ISBN/ISSN/Other

  • ISSN: 1090-0535