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2013 | 73 | 1 |

Tytuł artykułu

Object-based analysis of astroglial reaction and astrocyte subtype morphology after ischemic brain injury

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The astrocytic response to ischemic brain injury is characterized by specific alterations of glial cell morphology and function. Various studies described both beneficial and detrimental aspects of activated astrocytes, suggesting the existence of different subtypes. We investigated this issue using a novel object-based approach to study characteristics of astrogliosis after stroke. Spontaneously hypertensive rats received permanent middle cerebral artery occlusion. After 96 h, brain specimens were removed, fixed and stained for GFAP, glutaminę synthetase (GS), S100P and Musashil (Mshl). Three regions of interest were defined (contralateral hemisphere, ipsilateral remote zone and infarct border zone), and confocal stacks were acquired (n=5 biological with each n=4 technical replicates). The stacks were background-corrected and colocalization between the selected markers and GFAP was determined using an automated thresholding algorithm. The fluorescence and colocalization channels were then converted into 3D-objects using both intensity and volume as filters to ultimately determine the final volumes of marker expression and colocalization, as well as the morphological changes of astrocyte process arborisation. We found that both S100P and Mshl determined the same GFAP-positive astroglial cell population albeit the cellular compartments differed. GFAP stained most of the astrocyte processes and is hence suitable for the analysis of qualitative characteristics of astrogliosis. Due to its peri-nuclear localization, Mshl is appropriate to estimate the total number of astrocytes even in regions with severe reactive astrogliosis. GS expression in GFAP-positive astrocytes was high in the remote zone and low at the infarct border, indicating the existence of astrocyte subclasses.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

73

Numer

1

Opis fizyczny

p.79-87,fig.,ref.

Twórcy

autor
  • Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany
  • Translation Center for Regenerative Medicine, Leipzig, Germany
autor
  • Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany
autor
  • Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany
autor
  • Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany
  • Translation Center for Regenerative Medicine, Leipzig, Germany
autor
  • Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany
  • Translation Center for Regenerative Medicine, Leipzig, Germany
autor
  • Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany
  • Translation Center for Regenerative Medicine, Leipzig, Germany
  • Massachusetts General Hospital and Harvard Medical School, MA, USA
autor
  • Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany
  • Translation Center for Regenerative Medicine, Leipzig, Germany

Bibliografia

  • Baas D, Dalencon D, Fressinaud C, Vitkovic L, Sarlieve LL (1998) Oligodendrocyte-type-2 astrocyte (O-2A) progeni¬tor cells express glutamine synthetase: Developmental and cell type-specific regulation. Mol Psychiatry 3: 356-361.
  • Barreto GE, Sun X, Xu L, Giffard RG (2011) Astrocyte proliferation following stroke in the mouse depends on distance from the infarct. PLoS One 6: e27881.
  • Benesova J, Hock M, Butenko O, Prajerova I, Anderova M, Chvatal A (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.
  • Bolte S, Cordelieres FP (2006) A Guided tour into subcel¬lular colocalization analysis in light microscopy. J Microsc 224: 213-232.
  • Cammer W (1990) Glutamine synthetase in the central ner¬vous system is not confined to astrocytes. J Neuroimmunol 26: 173-178.
  • Comeau JW, Costantino S, Wiseman PW (2006) A guide to accurate fluorescence microscopy colocalization mea¬surements. Biophys J 91: 4611-4622.
  • Costes SV, Daelemans D, Cho EH, Dobbin Z, Pavlakis G, Lockett S (2004) Automatic and quantitative measure¬ment of protein-protein colocalization in live cells. Biophys J 86: 3993-4003.
  • Kim WR, Kim JY, Moon Y, Kim HJ, Kim H, Sun W (2012) Regional difference of reactive astrogliosis following traumatic brain injury revealed by HGFAP-GFP trans¬genic mice. Neurosci Lett 513: 155-159.
  • Kimelberg HK (2004) The problem of astrocyte identity. Neurochem Int 45: 191-202.
  • Liberto CM, Albrecht PJ, Herx LM, Yong VW, Levison SW (2004) Pro-regenerative properties of cytokine-activated astrocytes. J Neurochem 89: 1092-1100.
  • Manders EM, Stap J, Brakenhoff GJ, van DR, Aten JA (1992) Dynamics of three-dimensional replication pat¬terns during the S-phase, analysed by double labelling of DNA and confocal microscopy. J Cell Sci 103: 857-862.
  • Menet V, Prieto M, Privat A, Ribotta M (2003) Axonal plastic¬ity and functional recovery after spinal cord injury in mice deficient in both glial fibrillary acidic protein and vimentin genes. Proc Natl Acad Sci U S A 100: 8999-9004.
  • Okada S, Nakamura M, Katoh H, Miyao T, Shimazaki T, Ishii K, Yamane J, Yoshimura A, Iwamoto Y, Toyama Y, Okano H (2006) Conditional ablation of stat3 or socs3 discloses a dual role for reactive astrocytes after spinal cord injury. Nat Med 12: 829-834.
  • Oki K, Kaneko N, Kanki H, Imai T, Suzuki N, Sawamoto K, Okano H (2010) Musashil as a marker of reactive astro- cytes after transient focal brain ischemia. Neurosci Res 66: 390-395.
  • Paxinos G, Watson C (2006) The Rat Brain in Stereotaxic Coordinates (6th ed). Academic Press, New York, NY.
  • Popa-Wagner A, Buga AM, Kokaia Z (2011) Perturbed cel¬lular response to brain injury during aging. Ageing Res Rev 10: 71-79.
  • Riegelsberger UM, Deten A, Posel C, Zille M, Kranz A, Boltze J, Wagner DC (2011) Intravenous human umbili¬cal cord blood transplantation for stroke: impact on infarct volume and caspase-3-dependent cell death in spontaneously hypertensive rats. Exp Neurol 227: 218¬223.
  • Shimada IS, Borders A, Aronshtam A, Spees JL (2011) Proliferating reactive astrocytes are regulated by Notch-1 in the peri-infarct area after stroke. Stroke 42: 3231¬3237.
  • Silver J, Miller JH (2004) Regeneration beyond the glial scar. Nat Rev Neurosci 5: 146-156.
  • Singan VR, Jones TR, Curran KM, Simpson JC (2011) Dual channel rank-based intensity weighting for quantitative co-localization of microscopy images. BMC Bioinformatics 12: 407.
  • Sofroniew MV (2009) Molecular dissection of reactive astrogliosis and glial scar formation. Trends Neurosci 32: 638-647.
  • Sofroniew MV, Vinters HV (2010) Astrocytes: Biology and pathology. Acta Neuropathol 119: 7-35.
  • Stahlberg A, Andersson D, Aurelius J, Faiz M, Pekna M, Kubista M, Pekny M (2011) Defining Cell populations with single-cell gene expression profiling: Correlations and identification of astrocyte subpopulations. Nucleic Acids Res 39: e24.
  • Sun D, Jakobs TC (2012) Structural remodeling of astro¬cytes in the injured CNS. Neuroscientist 18: 567-588.
  • Takahashi H, Matsumoto H, Kumon Y, Ohnishi T, Freeman C, Imai Y, Tanaka J (2007) Expression of heparanase in nestin-positive reactive astrocytes in ischemic lesions of rat brain after transient middle cerebral artery occlusion. Neurosci Lett 417: 250-254.
  • Tanaka K, Nogawa S, Suzuki S, Dembo T, Kosakai A (2003) Upregulation of oligodendrocyte progenitor cells associ¬ated with restoration of mature oligodendrocytes and myelination in peri-infarct area in the rat brain. Brain Res 989: 172-179.
  • Walz W (2000) Controversy surrounding the existence of discrete functional classes of astrocytes in adult gray mat¬ter. Glia 31: 95-103.
  • Wang K, Walz W (2003) Unusual topographical pattern of proximal astrogliosis around a cortical devascularizing lesion. J Neurosci Res 73: 497-506.
  • Wang K, Bekar LK, Furber K, Walz W (2004) Vimentin- expressing proximal reactive astrocytes correlate with migration rather than proliferation following focal brain injury. Brain Res 1024: 193-202.
  • White RE, McTigue DM, Jakeman LB (2010) Regional het¬erogeneity in astrocyte responses following contusive spinal cord injury in mice. J Comp Neurol 518: 1370¬1390.
  • Wilhelmsson U, Li L, Pekna M, Berthold CH, Blom S, Eliasson C, Renner O, Bushong E, Ellisman M, Morgan TE, Pekny M (2004) Absence of glial fibrillary acidic protein and vimentin prevents hypertrophy of astrocytic processes and improves post-traumatic regeneration. J Neurosci 24: 5016-5021.
  • Wilhelmsson U, Bushong EA, Price DL, Smarr BL, Phung V, Terada M, Ellisman MH, Pekny M (2006) Redefining the concept of reactive astrocytes as cells that remain within their unique domains upon reaction to injury. Proc Natl Acad Sci U S A 103: 17513¬17518.
  • Zamanian JL, Xu L, Foo LC, Nouri N, Zhou L, Giffard RG, Barres BA (2012) Genomic analysis of reactive astroglio¬sis. J Neurosci 32: 6391-6410.
  • Zou J, Wang YX, Mu HJ, Xiang J, Wu W, Zhang B, Xie P (2011) Down-regulation of glutamine synthetase enhanc¬es migration of rat astrocytes after in vitro injury. Neurochem Int 58: 404-413.

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