The impact of alpha-syntrophin deletion on the changes in tissue structure and extracellular diffusion associated with cell swelling under physiological and pathological conditions
Jazyk angličtina Země Spojené státy americké Médium electronic-print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23861848
PubMed Central
PMC3702576
DOI
10.1371/journal.pone.0068044
PII: PONE-D-13-06265
Knihovny.cz E-zdroje
- MeSH
- akvaporin 4 metabolismus MeSH
- astrocyty metabolismus MeSH
- delece genu * MeSH
- difuze MeSH
- draslík metabolismus MeSH
- extracelulární prostor metabolismus MeSH
- genotyp MeSH
- genový knockout MeSH
- ischemie genetika MeSH
- membránové proteiny genetika metabolismus MeSH
- myši knockoutované MeSH
- myši MeSH
- osmotický tlak MeSH
- proteiny vázající vápník genetika metabolismus MeSH
- somatosenzorické korové centrum metabolismus MeSH
- srdeční zástava genetika metabolismus MeSH
- svalové proteiny genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- akvaporin 4 MeSH
- draslík MeSH
- membránové proteiny MeSH
- proteiny vázající vápník MeSH
- svalové proteiny MeSH
- syntrophin alpha1 MeSH Prohlížeč
Aquaporin-4 (AQP4) is the primary cellular water channel in the brain and is abundantly expressed by astrocytes along the blood-brain barrier and brain-cerebrospinal fluid interfaces. Water transport via AQP4 contributes to the activity-dependent volume changes of the extracellular space (ECS), which affect extracellular solute concentrations and neuronal excitability. AQP4 is anchored by α-syntrophin (α-syn), the deletion of which leads to reduced AQP4 levels in perivascular and subpial membranes. We used the real-time iontophoretic method and/or diffusion-weighted magnetic resonance imaging to clarify the impact of α-syn deletion on astrocyte morphology and changes in extracellular diffusion associated with cell swelling in vitro and in vivo. In mice lacking α-syn, we found higher resting values of the apparent diffusion coefficient of water (ADCW) and the extracellular volume fraction (α). No significant differences in tortuosity (λ) or non-specific uptake (k'), were found between α-syn-negative (α-syn -/-) and α-syn-positive (α-syn +/+) mice. The deletion of α-syn resulted in a significantly smaller relative decrease in α observed during elevated K(+) (10 mM) and severe hypotonic stress (-100 mOsmol/l), but not during mild hypotonic stress (-50 mOsmol/l). After the induction of terminal ischemia/anoxia, the final values of ADCW as well as of the ECS volume fraction α indicate milder cell swelling in α-syn -/- in comparison with α-syn +/+ mice. Shortly after terminal ischemia/anoxia induction, the onset of a steep rise in the extracellular potassium concentration and an increase in λ was faster in α-syn -/- mice, but the final values did not differ between α-syn -/- and α-syn +/+ mice. This study reveals that water transport through AQP4 channels enhances and accelerates astrocyte swelling. The substantially altered ECS diffusion parameters will likely affect the movement of neuroactive substances and/or trophic factors, which in turn may modulate the extent of tissue damage and/or drug distribution.
Zobrazit více v PubMed
Sykova E (1997) The extracellular space in the CNS: its regulation, volume and geometry in normal and pathological neuronal function. The Neuroscientist: 28–41.
Magistretti PJ, Pellerin L (2000) The astrocyte-mediated coupling between synaptic activity and energy metabolism operates through volume transmission. Prog Brain Res 125: 229–240. PubMed
Vajda Z, Promeneur D, Doczi T, Sulyok E, Frokiaer J, et al. (2000) Increased aquaporin-4 immunoreactivity in rat brain in response to systemic hyponatremia. Biochem Biophys Res Commun 270: 495–503. PubMed
Taniguchi M, Yamashita T, Kumura E, Tamatani M, Kobayashi A, et al. (2000) Induction of aquaporin-4 water channel mRNA after focal cerebral ischemia in rat. Brain Res Mol Brain Res 78: 131–137. PubMed
Ke C, Poon WS, Ng HK, Pang JC, Chan Y (2001) Heterogeneous responses of aquaporin-4 in oedema formation in a replicated severe traumatic brain injury model in rats. Neurosci Lett 301: 21–24. PubMed
Frydenlund DS, Bhardwaj A, Otsuka T, Mylonakou MN, Yasumura T, et al. (2006) Temporary loss of perivascular aquaporin-4 in neocortex after transient middle cerebral artery occlusion in mice. Proc Natl Acad Sci U S A 103: 13532–13536. PubMed PMC
Solenov E, Watanabe H, Manley GT, Verkman AS (2004) Sevenfold-reduced osmotic water permeability in primary astrocyte cultures from AQP-4-deficient mice, measured by a fluorescence quenching method. Am J Physiol Cell Physiol 286: C426–432. PubMed
Neely JD, Amiry-Moghaddam M, Ottersen OP, Froehner SC, Agre P, et al. (2001) Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein. Proc Natl Acad Sci U S A 98: 14108–14113. PubMed PMC
Amiry-Moghaddam M, Williamson A, Palomba M, Eid T, de Lanerolle NC, et al. (2003) Delayed K+ clearance associated with aquaporin-4 mislocalization: phenotypic defects in brains of alpha-syntrophin-null mice. Proc Natl Acad Sci U S A 100: 13615–13620. PubMed PMC
Amiry-Moghaddam M, Frydenlund DS, Ottersen OP (2004) Anchoring of aquaporin-4 in brain: molecular mechanisms and implications for the physiology and pathophysiology of water transport. Neuroscience 129: 999–1010. PubMed
Binder DK, Yao X, Zador Z, Sick TJ, Verkman AS, et al. (2006) Increased seizure duration and slowed potassium kinetics in mice lacking aquaporin-4 water channels. Glia 53: 631–636. PubMed
Strohschein S, Huttmann K, Gabriel S, Binder DK, Heinemann U, et al. (2011) Impact of aquaporin-4 channels on K+ buffering and gap junction coupling in the hippocampus. Glia 59: 973–980. PubMed
Manley GT, Fujimura M, Ma T, Noshita N, Filiz F, et al. (2000) Aquaporin-4 deletion in mice reduces brain edema after acute water intoxication and ischemic stroke. Nat Med 6: 159–163. PubMed
Papadopoulos MC, Verkman AS (2005) Aquaporin-4 gene disruption in mice reduces brain swelling and mortality in pneumococcal meningitis. J Biol Chem 280: 13906–13912. PubMed
Binder DK, Oshio K, Ma T, Verkman AS, Manley GT (2004) Increased seizure threshold in mice lacking aquaporin-4 water channels. Neuroreport 15: 259–262. PubMed
Binder DK, Nagelhus EA, Ottersen OP (2012) Aquaporin-4 and epilepsy. Glia 60: 1203–1214. PubMed
Bloch O, Papadopoulos MC, Manley GT, Verkman AS (2005) Aquaporin-4 gene deletion in mice increases focal edema associated with staphylococcal brain abscess. J Neurochem 95: 254–262. PubMed
Bloch O, Auguste KI, Manley GT, Verkman AS (2006) Accelerated progression of kaolin-induced hydrocephalus in aquaporin-4-deficient mice. J Cereb Blood Flow Metab 26: 1527–1537. PubMed
Verkman AS (2012) Aquaporins in clinical medicine. Annu Rev Med 63: 303–316. PubMed PMC
Nicholson C, Sykova E (1998) Extracellular space structure revealed by diffusion analysis. Trends Neurosci 21: 207–215. PubMed
Sykova E, Nicholson C (2008) Diffusion in brain extracellular space. Physiol Rev 88: 1277–1340. PubMed PMC
Nicholson C, Phillips JM (1981) Ion diffusion modified by tortuosity and volume fraction in the extracellular microenvironment of the rat cerebellum. J Physiol 321: 225–257. PubMed PMC
Sykova E (1992) Ion-selective electrodes. In: York SJN, editor. Monitoring neuronal activity: a practical approach: Oxford Univ. Press. 261–282.
Svoboda J, Sykova E (1991) Extracellular space volume changes in the rat spinal cord produced by nerve stimulation and peripheral injury. Brain Res 560: 216–224. PubMed
Franklin KBJ, Paxinos G (1997) The Mouse Brain in Stereotaxic Coordinates. San Diego: Academic Press.
Yao X, Hrabetova S, Nicholson C, Manley GT (2008) Aquaporin-4-deficient mice have increased extracellular space without tortuosity change. J Neurosci 28: 5460–5464. PubMed PMC
Amiry-Moghaddam M, Otsuka T, Hurn PD, Traystman RJ, Haug FM, et al. (2003) An alpha-syntrophin-dependent pool of AQP4 in astroglial end-feet confers bidirectional water flow between blood and brain. Proc Natl Acad Sci U S A 100: 2106–2111. PubMed PMC
Zeynalov E, Chen CH, Froehner SC, Adams ME, Ottersen OP, et al. (2008) The perivascular pool of aquaporin-4 mediates the effect of osmotherapy in postischemic cerebral edema. Crit Care Med 36: 2634–2640. PubMed PMC
Haj-Yasein NN, Vindedal GF, Eilert-Olsen M, Gundersen GA, Skare O, et al. (2011) Glial-conditional deletion of aquaporin-4 (Aqp4) reduces blood-brain water uptake and confers barrier function on perivascular astrocyte endfeet. Proc Natl Acad Sci U S A 108: 17815–17820. PubMed PMC
Papadopoulos MC, Binder DK, Verkman AS (2005) Enhanced macromolecular diffusion in brain extracellular space in mouse models of vasogenic edema measured by cortical surface photobleaching. FASEB J 19: 425–427. PubMed
Zador Z, Magzoub M, Jin S, Manley GT, Papadopoulos MC, et al. (2008) Microfiberoptic fluorescence photobleaching reveals size-dependent macromolecule diffusion in extracellular space deep in brain. FASEB J 22: 870–879. PubMed
Xiao F, Hrabetova S (2009) Enlarged extracellular space of aquaporin-4-deficient mice does not enhance diffusion of Alexa Fluor 488 or dextran polymers. Neuroscience 161: 39–45. PubMed PMC
Vorisek I, Sykova E (2009) Measuring diffusion parameters in the brain: comparing the real-time iontophoretic method and diffusion-weighted magnetic resonance. Acta Physiol (Oxf) 195: 101–110. PubMed
Kimelberg HK, Rutledge E, Goderie S, Charniga C (1995) Astrocytic swelling due to hypotonic or high K+ medium causes inhibition of glutamate and aspartate uptake and increases their release. J Cereb Blood Flow Metab 15: 409–416. PubMed
Su G, Kintner DB, Sun D (2002) Contribution of Na(+)-K(+)-Cl(−) cotransporter to high-[K(+)](o)- induced swelling and EAA release in astrocytes. Am J Physiol Cell Physiol 282: C1136–1146. PubMed
Benesova J, Hock M, Butenko O, Prajerova I, Anderova M, et al. (2009) Quantification of astrocyte volume changes during ischemia in situ reveals two populations of astrocytes in the cortex of GFAP/EGFP mice. J Neurosci Res 87: 96–111. PubMed
Pivonkova H, Benesova J, Butenko O, Chvatal A, Anderova M (2010) Impact of global cerebral ischemia on K+ channel expression and membrane properties of glial cells in the rat hippocampus. Neurochem Int 57: 783–794. PubMed
Vorisek I, Sykova E (1997) Ischemia-induced changes in the extracellular space diffusion parameters, K+, and pH in the developing rat cortex and corpus callosum. J Cereb Blood Flow Metab 17: 191–203. PubMed
Guadagno E, Moukhles H (2004) Laminin-induced aggregation of the inwardly rectifying potassium channel, Kir4.1, and the water-permeable channel, AQP4, via a dystroglycan-containing complex in astrocytes. Glia 47: 138–149. PubMed
Connors NC, Adams ME, Froehner SC, Kofuji P (2004) The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia. J Biol Chem 279: 28387–28392. PubMed
Nagelhus EA, Mathiisen TM, Ottersen OP (2004) Aquaporin-4 in the central nervous system: cellular and subcellular distribution and coexpression with KIR4.1. Neuroscience 129: 905–913. PubMed
Nagelhus EA, Horio Y, Inanobe A, Fujita A, Haug FM, et al. (1999) Immunogold evidence suggests that coupling of K+ siphoning and water transport in rat retinal Muller cells is mediated by a coenrichment of Kir4.1 and AQP4 in specific membrane domains. Glia 26: 47–54. PubMed
Zhang H, Verkman AS (2008) Aquaporin-4 independent Kir4.1 K+ channel function in brain glial cells. Mol Cell Neurosci 37: 1–10. PubMed PMC
Haj-Yasein NN, Jensen V, Vindedal GF, Gundersen GA, Klungland A, et al. (2011) Evidence that compromised K+ spatial buffering contributes to the epileptogenic effect of mutations in the human Kir4.1 gene (KCNJ10). Glia 59: 1635–1642. PubMed
Sykova E, Vargova L, Prokopova S, Simonova Z (1999) Glial swelling and astrogliosis produce diffusion barriers in the rat spinal cord. Glia 25: 56–70. PubMed
Neprasova H, Anderova M, Petrik D, Vargova L, Kubinova S, et al. (2007) High extracellular K(+) evokes changes in voltage-dependent K(+) and Na (+) currents and volume regulation in astrocytes. Pflugers Arch 453: 839–849. PubMed
Altered astrocytic swelling in the cortex of α-syntrophin-negative GFAP/EGFP mice
Astrocytes and extracellular matrix in extrasynaptic volume transmission