4.6 Article

Brain water mobility decreases after astrocytic aquaporin-4 inhibition using RNA interference

Journal

JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM
Volume 31, Issue 3, Pages 819-831

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1038/jcbfm.2010.163

Keywords

apparent diffusion coefficient; edema; neuroimaging; neurovascular unit; water channel

Funding

  1. Swiss Science Foundation [FN 3100AO-108001, 31003A-122166, IZK0Z3-128973]
  2. NIH, Department of Pediatrics [R01HD061946]
  3. NASA [NCC9-149]
  4. Swiss National Science Foundation (SNF) [IZK0Z3_128973, 31003A-122166] Funding Source: Swiss National Science Foundation (SNF)

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Neuroimaging with diffusion-weighted imaging is routinely used for clinical diagnosis/prognosis. Its quantitative parameter, the apparent diffusion coefficient (ADC), is thought to reflect water mobility in brain tissues. After injury, reduced ADC values are thought to be secondary to decreases in the extracellular space caused by cell swelling. However, the physiological mechanisms associated with such changes remain uncertain. Aquaporins (AQPs) facilitate water diffusion through the plasma membrane and provide a unique opportunity to examine the molecular mechanisms underlying water mobility. Because of this critical role and the recognition that brain AQP4 is distributed within astrocytic cell membranes, we hypothesized that AQP4 contributes to the regulation of water diffusion and variations in its expression would alter ADC values in normal brain. Using RNA interference in the rodent brain, we acutely knocked down AQP4 expression and observed that a 27% AQP4-specific silencing induced a 50% decrease in ADC values, without modification of tissue histology. Our results demonstrate that ADC values in normal brain are modulated by astrocytic AQP4. These findings have major clinical relevance as they suggest that imaging changes seen in acute neurologic disorders such as stroke and trauma are in part due to changes in tissue AQP4 levels. Journal of Cerebral Blood Flow & Metabolism (2011) 31, 819-831; doi:10.1038/jcbfm.2010.163; published online 29 September 2010

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