Astrocytes specifically remove surface-adsorbed fibrinogen and locally express chondroitin sulfate proteoglycans

Acta Biomaterialia

Volumn 9, Issue 7, 2013, Pages 7200-7208

  Hsiao, Tony W ^a   Swarup, Vimal P ^a   Kuberan, Balagurunathan ^b   Tresco, Patrick A ^a   Hlady, Vladimir ^a  

^a University of Utah   (United States)

^b UNIVERSITY OF UTAH   (United States)

Author keywords

Astrocytes; Chondroitin sulfate proteoglycan; Fibrinogen; TGF ; TGF inhibitor SB 431542

Indexed keywords

PROTEINS; SULFUR COMPOUNDS;

ASTROCYTE; CHONDROITIN SULFATE PROTEOGLYCANS; FIBRINOGEN; IN-VITRO; REMOVAL PROCESS; TRANSFORMING GROWTH FACTOR TYPE Β; TRANSFORMING GROWTH FACTOR TYPE Β INHIBITOR SB 431542; TRANSFORMING GROWTH FACTORS; TWO PHASE;

CELL SIGNALING;

4 [4 (1,3 BENZODIOXOL 5 YL) 5 (2 PYRIDINYL) 1H IMIDAZOL 2 YL]BENZAMIDE; FIBRINOGEN; PLASMA PROTEIN; PROTEOCHONDROITIN SULFATE; SULFUR 35; TRANSFORMING GROWTH FACTOR BETA;

ADHERENT CELL; ADSORPTION; ANIMAL CELL; ARTICLE; ASTROCYTE; ASTROCYTOSIS; CELL MEMBRANE; CONTROLLED STUDY; EPILEPTOGENESIS; GLYCOPROTEIN SYNTHESIS; IMMUNOCYTOCHEMISTRY; IN VITRO STUDY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; RADIOACTIVITY;

EID: 84878282568     PISSN: 17427061     EISSN: 18787568     Source Type: Journal    
DOI: 10.1016/j.actbio.2013.02.047     Document Type: Article

References (31)

1. B.D. Winslow, and P.A. Tresco Quantitative analysis of the tissue response to chronically implanted microwire electrodes in rat cortex Biomaterials 31 2010 1558 1567
2. R. Biran, D.C. Martin, and P.A. Tresco Neuronal cell loss accompanies the brain tissue response to chronically implanted silicon microelectrode arrays Exp Neurol 195 2005 115 126
3. V.S. Polikov, P.A. Tresco, and W.M. Reichert Response of brain tissue to chronically implanted neural electrodes J Neurosci Methods 148 2005 1 18
4. J.L. Brash The fate of fibrinogen following adsorption at the blood-biomaterial, interface Ann NY Acad Sci 516 1987 206 222
5. P. Roach, D. Farrar, and C.C. Perry Interpretation of protein adsorption: surface-induced conformational changes J Am Chem Soc 127 2005 8168 8173
6. M.V. Sofroniew Molecular dissection of reactive astrogliosis and glial scar formation Trends Neurosci 32 2009 638 647
7. E. East, J.P. Golding, and J.B. Phillips A versatile 3D culture model facilitates monitoring of astrocytes undergoing reactive gliosis J Tissue Eng Regener Med 3 2009 634 646
8. S.J.A. Davies, D.R. Goucher, C. Doller, and J. Silver Robust regeneration of adult sensory axons in degenerating white matter of the adult rat spinal cord J Neurosci 19 1999 5810 5822
9. K.E. Dow, and W. Wang Cell biology of astrocyte proteoglycans Cell Mol Life Sci 54 1998 567 581
10. H. Yamada, B. Fredette, K. Shitara, K. Hagihara, R. Miura, and B. Ranscht The brain chondroitin sulfate proteoglycan brevican associates with astrocytes ensheathing cerebellar glomeruli and inhibits neurite outgrowth from granule neurons J Neurosci 17 1997 7784 7795
11. R.A. Asher, D.A. Morgenstern, P.S. Fidler, K.H. Adcock, A. Oohira, and J.E. Braistead Neurocan is upregulated in injured brain and in cytokine-treated astrocytes J Neurosci 20 2000 2427 2438
12. J. Silver, and J.H. Miller Regeneration beyond the glial scar Nat Rev Neurosci 5 2004 146 156
13. G.M. Smith, and C. Strunz Growth factor and cytokine regulation of chondroitin sulfate proteoglycans by astrocytes Glia 52 2005 209 218
14. J. Kimura-Kuroda, X. Teng, Y. Komuta, N. Yoshioka, K. Sango, and K. Kawamura An in vitro model of the inhibition of axon growth in the lesion scar formed after central nervous system injury Mol Cell Neurosci 43 2010 177 187
15. C. Schachtrup, J.K. Ryu, M.J. Helmrick, E. Vagena, D.K. Galanakis, and J.L. Degen Fibrinogen triggers astrocyte scar formation by promoting the availability of active TGF-β after vascular damage J Neurosci 30 2010 5843 5854
16. J.P. O'Callaghan, D.B. Miller, and J.F. Reinhard Jr. Characterization of the origins of astrocyte response to injury using the dopaminergic neurotoxicant, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine Brain Res 521 1990 73 80
17. K.D. McCarthy, and J. de Vellis Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue J Cell Biol 85 1980 890 902
18. L.E. Corum, C.D. Eichinger, T.W. Hsiao, and V. Hlady Using microcontact printing of fibrinogen to control surface-induced platelet adhesion and activation Langmuir 27 2011 8316 8322
19. Y. Xia, and G.M. Whitesides Soft lithography Annu Rev Mater Sci 28 1998 153 184
20. X.V. Victor, T.K.N. Nguyen, M. Ethirajan, V.M. Tran, K.V. Nguyen, and B. Kuberan Investigating the elusive mechanism of glycosaminoglycan biosynthesis J Biol Chem 284 2009 25842 25853
21. S.K.R. Pixley, M. Nieto-Sampedro, and C.W. Cotman Preferential adhesion of brain astrocytes to laminin and central neurites to astrocytes J Neurosci Res 18 1987 402 406
22. G.J. Inman, F.J. Nicolás, J.F. Callahan, J.D. Harling, L.M. Gaster, and A.D. Reith SB-431542 is a potent and specific inhibitor of transforming growth factor-β superfamily type I activin receptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7 Mol Pharmacol 62 2002 65 74
23. A. Friedman, D. Kaufer, and U. Heinemann Blood-brain barrier breakdown-inducing astrocytic transformation: novel targets for the prevention of epilepsy Epilepsy Res 85 2009 142 149
24. S. Ivens, D. Kaufer, L.P. Flores, I. Bechmann, D. Zumsteg, and O. Tomkins TGF-β receptor-mediated albumin uptake into astrocytes is involved in neocortical epileptogenesis Brain 130 2007 535 547
25. M.L. Condic, D.M. Snow, and P.C. Letourneau Embryonic neurons adapt to the inhibitory proteoglycan aggrecan by increasing integrin expression J Neurosci 19 1999 10036 10043
26. D.M. Snow, J.D. Smith, and J.A. Gurwell Binding characteristics of chondroitin sulfate proteoglycans and laminin-1, and correlative neurite outgrowth behaviors in a standard tissue culture choice assay J Neurobiol 51 2002 285 301
27. X. Tang, J.E. Davies, and S.J.A. Davies Changes in distribution, cell associations, and protein expression levels of NG2, neurocan, phosphacan, brevican, versican V2, and tenascin-C during acute to chronic maturation of spinal cord scar tissue J Neurosci Res 71 2003 427 444
28. C. Lagord, M. Berry, and A. Logan Expression of TGFβ2 but not TGFβ1 correlates with the deposition of scar tissue in the lesioned spinal cord Mol Cell Neurosci 20 2002 69 92
29. E.J. Bradbury, L.D.F. Moon, R.J. Popat, V.R. King, G.S. Bennett, and P.N. Patel Chondroitinase ABC promotes functional recovery after spinal cord injury Nature 416 2002 636 640
30. W.J. Alilain, K.P. Horn, H. Hu, T.E. Dick, and J. Silver Functional regeneration of respiratory pathways after spinal cord injury Nature 475 2011 196 200
31. K. Beck, and C. Schachtrup Vascular damage in the central nervous system: a multifaceted role for vascular-derived TGF-β Cell Tissue Res 347 2012 187 201