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  1. Article ; Online: Loss of connexin36 in rat hippocampus and cerebellar cortex in persistent Borna disease virus infection.

    Köster-Patzlaff, Christiane / Hosseini, Seyed Mehdi / Reuss, Bernhard

    Journal of chemical neuroanatomy

    2008  Volume 37, Issue 2, Page(s) 118–127

    Abstract: Neonatal Borna disease virus (BDV) infection of the Lewis rat leads to progressive degeneration of dentate gyrus granule cells, and cerebellar Purkinje neurons. Our aim here was to clarify whether BDV interfered with the formation of electrical synapses, ...

    Abstract Neonatal Borna disease virus (BDV) infection of the Lewis rat leads to progressive degeneration of dentate gyrus granule cells, and cerebellar Purkinje neurons. Our aim here was to clarify whether BDV interfered with the formation of electrical synapses, and we, therefore, analysed expression of the neuronal gap junction protein connexin36 (Cx36) in the Lewis rat hippocampal formation, and cerebellar cortex, 4 and 8 weeks after neonatal infection. Semiquantitative RT-PCR, revealed a BDV-dependent decrease in Cx36 mRNA in the hippocampal formation 4 and 8 weeks post-infection (p.i.), and in the cerebellar cortex 8 weeks p.i. Correspondingly, immunofluorescent staining revealed reduced Cx36 immunoreactivity in both dentate gyrus, and ammons horn CA3 region, 4 and 8 weeks post-infection. In the cerebellar cortex, Cx36 immunoreactivity was detected only 8 weeks post-infection in the molecular layer, where it was down regulated by BDV. Our findings demonstrate, for the first time, distinct BDV-dependent reductions in Cx36 mRNA and protein in the rat hippocampal formation and cerebellar cortex, suggesting altered neuronal network properties to be an important feature of persistent viral brain infections.
    MeSH term(s) Age Factors ; Animals ; Animals, Newborn ; Borna Disease/metabolism ; Borna Disease/pathology ; Borna Disease/physiopathology ; Cerebellar Cortex/metabolism ; Cerebellar Cortex/physiopathology ; Cerebellar Cortex/virology ; Connexins/genetics ; Down-Regulation/physiology ; Female ; Fluorescent Antibody Technique ; Gap Junctions/metabolism ; Gap Junctions/pathology ; Gene Expression Regulation/physiology ; Hippocampus/metabolism ; Hippocampus/physiopathology ; Hippocampus/virology ; Nerve Degeneration/metabolism ; Nerve Degeneration/physiopathology ; Nerve Degeneration/virology ; Nerve Net/metabolism ; Nerve Net/physiopathology ; Nerve Net/virology ; RNA, Messenger/metabolism ; Rats ; Rats, Inbred Lew ; Synaptic Transmission/physiology ; Gap Junction delta-2 Protein
    Chemical Substances Connexins ; RNA, Messenger
    Language English
    Publishing date 2008-11-07
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639443-7
    ISSN 1873-6300 ; 0891-0618
    ISSN (online) 1873-6300
    ISSN 0891-0618
    DOI 10.1016/j.jchemneu.2008.10.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Layer specific changes of astroglial gap junctions in the rat cerebellar cortex by persistent Borna Disease Virus infection.

    Köster-Patzlaff, Christiane / Hosseini, Seyed Mehdi / Reuss, Bernhard

    Brain research

    2008  Volume 1219, Page(s) 143–158

    Abstract: Neonatal Borna Disease Virus (BDV) infection of the Lewis rat brain, leads to Purkinje cell degeneration, in association with astroglial activation. Since astroglial gap junctions (GJ) are known to influence neuronal degeneration, we investigated BDV ... ...

    Abstract Neonatal Borna Disease Virus (BDV) infection of the Lewis rat brain, leads to Purkinje cell degeneration, in association with astroglial activation. Since astroglial gap junctions (GJ) are known to influence neuronal degeneration, we investigated BDV dependent changes in astroglial GJ connexins (Cx) Cx43, and Cx30 in the Lewis rat cerebellum, 4, and 8 weeks after neonatal infection. On the mRNA level, RT-PCR demonstrated a BDV dependent increase in cerebellar Cx43, and a decrease in Cx30, 8, but not 4 weeks p.i. On the protein level, Western blot analysis revealed no overall upregulation of Cx43, but an increase of its phosphorylated forms, 8 weeks p.i. Cx30 protein was downregulated. Immunohistochemistry revealed a BDV dependent reduction of Cx43 in the granular layer (GL), 4 weeks p.i. 8 weeks p.i., Cx43 immunoreactivity recovered in the GL, and was induced in the molecular layer (ML). Cx30 revealed a BDV dependent decrease in the GL, both 4, and 8 weeks p.i. Changes in astroglial Cxs correlated not with expression of the astrogliotic marker GFAP, which was upregulated in radial glia. With regard to functional coupling, primary cerebellar astroglial cultures, revealed a BDV dependent increase of Cx43, and Cx30 immunoreactivity and in spreading of the GJ permeant dye Lucifer Yellow. These results demonstrate a massive, BDV dependent reorganization of astroglial Cx expression, and of functional GJ coupling in the cerebellar cortex, which might be of importance for the BDV dependent neurodegeneration in this brain region.
    MeSH term(s) Animals ; Animals, Newborn ; Borna Disease/pathology ; Borna Disease/virology ; Borna disease virus/pathogenicity ; Cells, Cultured ; Cerebellar Cortex/pathology ; Connexin 30 ; Connexin 43/genetics ; Connexin 43/metabolism ; Connexins/genetics ; Connexins/metabolism ; Disease Models, Animal ; Female ; Gap Junctions/pathology ; Gap Junctions/virology ; Gene Expression Regulation, Viral/physiology ; Glial Fibrillary Acidic Protein ; Male ; Neuroglia/metabolism ; Neuroglia/pathology ; Neuroglia/virology ; Pregnancy ; RNA, Messenger/metabolism ; Rats ; Rats, Inbred Lew ; Time Factors
    Chemical Substances Connexin 30 ; Connexin 43 ; Connexins ; Gjb6 protein, rat ; Glial Fibrillary Acidic Protein ; RNA, Messenger
    Language English
    Publishing date 2008-07-11
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1200-2
    ISSN 1872-6240 ; 0006-8993
    ISSN (online) 1872-6240
    ISSN 0006-8993
    DOI 10.1016/j.brainres.2008.04.062
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book ; Thesis: Klonierung und Charakterisierung des Interleukin-1[beta]-Systems im Gehirn von Callithrix jacchus

    Köster-Patzlaff, Christiane

    2003  

    Author's details vorgelegt von Christiane Köster-Patzlaff
    Language German
    Size IV, 133 Bl, Ill., graph. Darst
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Univ., Diss.--Göttingen, 2003
    Note Auch als elektronisches Dokument vorh.
    Database Former special subject collection: coastal and deep sea fishing

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  4. Book ; Online ; Thesis: Klonierung und Charakterisierung des Interleukin-1β-Systems [Interleukin-1-Beta-Systems] im Gehirn von Callithrix jacchus

    Köster-Patzlaff, Christiane [Verfasser]

    2003  

    Author's details vorgelegt von Christiane Köster-Patzlaff, geb. Köster
    Keywords Medizin, Gesundheit ; Medicine, Health
    Subject code sg610
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  5. Book ; Online ; Thesis: Klonierung und Charakterisierung des Interleukin-1beta-Systems im Gehirn von Callithrix jacchus

    Köster-Patzlaff, Christiane

    Cloning and characterization of the interleukin-1beta-system in the brain of Callithrix jacchus

    2003  

    Abstract: As a new animal model for investigation of the interleukin-1b-system in the brain the species of non-human primates Callithrix jacchus was chosen.In this thesis the influence of artificial stress with lipopolysaccharid (LPS) and its effect on cytokines ... ...

    Title variant Cloning and characterization of the interleukin-1beta-system in the brain of Callithrix jacchus
    Author's details von Christiane Köster-Patzlaff
    Abstract As a new animal model for investigation of the interleukin-1b-system in the brain the species of non-human primates Callithrix jacchus was chosen.In this thesis the influence of artificial stress with lipopolysaccharid (LPS) and its effect on cytokines and the hormones in C. jacchus was investigate for the first time. The stimulating effect of the LPS-dose was pointed out clearly by the investigation of the stress hormones and cytokines. A reliable method of investigation (partial sequences) of the interleukin-1 systemcomponents in the brain of C. jacchus could have been developed. With that a proof of IL-1 systemcomponents under basal conditions was succeeded
    Language German
    Size Online-Ressource
    Edition Electronic edition
    Publisher Niedersächsische Staats- und Universitätsbibliothek
    Publishing place Göttingen
    Document type Book ; Online ; Thesis
    Thesis / German Habilitation thesis Univ., Diss.--Göttingen, 2003
    Database Former special subject collection: coastal and deep sea fishing

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  6. Article: Persistent Borna Disease Virus infection changes expression and function of astroglial gap junctions in vivo and in vitro.

    Köster-Patzlaff, Christiane / Hosseini, Seyed Mehdi / Reuss, Bernhard

    Brain research

    2007  Volume 1184, Page(s) 316–332

    Abstract: Neonatal Borna Disease Virus (BDV) infection of the Lewis rat brain leads to dentate gyrus (DG) degeneration, underlying mechanisms are not fully understood. Since astroglial gap junction (GJ) coupling is known to influence neurodegenerative processes, ... ...

    Abstract Neonatal Borna Disease Virus (BDV) infection of the Lewis rat brain leads to dentate gyrus (DG) degeneration, underlying mechanisms are not fully understood. Since astroglial gap junction (GJ) coupling is known to influence neurodegenerative processes, the question arose whether persistent BDV infection influences astroglial connexins (Cx) Cx43 and Cx30 in the hippocampal formation (HiF) of Lewis rats. RT-PCR and Western blot analysis of forebrain (FB) samples revealed a virus dependent reduction of both Cx types 8 but not 4 weeks post infection (p.i.). Immunohistochemistry revealed an increase of Cx43 in the DG and a decrease in the CA3 region 4 and 8 weeks p.i. Cx30, which was detectable only 8 weeks p.i., revealed a BDV dependent increase in DG and CA3 regions. BDV dependent astrogliosis as revealed by immunodetection of glial fibrillary acidic protein (GFAP) correlated not with astroglial connexin expression. With regard to functional coupling as revealed by scrape loading, BDV infection resulted in increased spreading of the GJ permeant dye Lucifer yellow in primary hippocampal astroglial cultures, and in increased expression of Cx43 and Cx30 as revealed by immunocytochemistry. In conclusion, persistent BDV infection of the Lewis rat brain leads to changes in astroglial Cx expression both in vivo and in vitro and of functional coupling in vitro. Distribution and time course of these changes suggest them to be a direct result of neurodegeneration in the DG and an indirect effect of neuronal deafferentiation in the CA3 region.
    MeSH term(s) Age Factors ; Animals ; Borna disease virus/pathogenicity ; Brain Diseases/pathology ; Brain Diseases/virology ; Connexin 43/genetics ; Connexin 43/metabolism ; Female ; Gap Junctions/metabolism ; Gene Expression Regulation, Viral/physiology ; Glial Fibrillary Acidic Protein ; Hippocampus/pathology ; In Vitro Techniques ; Neuroglia/metabolism ; Neuroglia/virology ; Pregnancy ; Rats ; Rats, Inbred Lew ; Viral Proteins/metabolism
    Chemical Substances Connexin 43 ; Glial Fibrillary Acidic Protein ; Viral Proteins ; p40 protein, Borna disease virus (148998-61-2)
    Language English
    Publishing date 2007-12-12
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1200-2
    ISSN 1872-6240 ; 0006-8993
    ISSN (online) 1872-6240
    ISSN 0006-8993
    DOI 10.1016/j.brainres.2007.09.062
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The colayer method as an efficient way to genetically modify mesencephalic progenitor cells transplanted into 6-OHDA rat model of Parkinson's disease.

    Ratzka, Andreas / Kalve, Ieva / Özer, Meltem / Nobre, André / Wesemann, Maike / Jungnickel, Julia / Köster-Patzlaff, Christiane / Baron, Olga / Grothe, Claudia

    Cell transplantation

    2012  Volume 21, Issue 4, Page(s) 749–762

    Abstract: Exogenous cell replacement represents a potent treatment option for Parkinson's disease. However, the low survival rate of transplanted dopaminergic neurons (DA) calls for methodological improvements. Here we evaluated a method to combine transient ... ...

    Abstract Exogenous cell replacement represents a potent treatment option for Parkinson's disease. However, the low survival rate of transplanted dopaminergic neurons (DA) calls for methodological improvements. Here we evaluated a method to combine transient genetic modification of neuronal progenitor cells with an optimized cell culture protocol prior to intrastriatal transplantation into 6-hydroxydopamine (6-OHDA) unilateral lesioned rats. Plasmid-based delivery of brain-derived neurotrophic factor (BDNF) increases the number of DA neurons, identified by tyrosine hydroxylase immunoreactivity (TH-ir), by 25% in vitro, compared to enhanced green fluorescence protein (EGFP)-transfected controls. However, the nucleofection itself, especially the cell detachment and reseeding procedure, decreases the TH-ir neuron number to 40% compared with nontransfected control cultures. To circumvent this drawback we established the colayer method, which contains a mix of nucleofected cells reseeded on top of an adherent sister culture in a ratio 1:3. In this setup TH-ir neuron number remains high and could be further increased by 25% after BDNF transfection. Comparison of both cell culture procedures (standard and colayer) after intrastriatal transplantation revealed a similar DA neuron survival as seen in vitro. Two weeks after grafting TH-ir neuron number was strongly reduced in animals receiving the standard EGFP-transfected cells (271 ± 62) compared to 1,723 ± 199 TH-ir neurons in the colayer group. In contrast to the in vitro results, no differences in the number of grafted TH-ir neurons were observed between BDNF, EGFP, and nontransfected colayer groups, neither 2 nor 13 weeks after transplantation. Likewise, amphetamine and apomorphine-induced rotational behavior improved similarly over time in all groups. Nevertheless, the colayer protocol provides an efficient way for neurotrophic factor release by transplanted progenitor cells and will help to study the effects of candidate factors on survival and integration of transplanted DA neurons.
    MeSH term(s) Animals ; Blotting, Western ; Brain-Derived Neurotrophic Factor/genetics ; Brain-Derived Neurotrophic Factor/metabolism ; Cells, Cultured ; Dopaminergic Neurons/cytology ; Dopaminergic Neurons/metabolism ; Green Fluorescent Proteins/genetics ; Green Fluorescent Proteins/metabolism ; Mesencephalon/cytology ; Oxidopamine/adverse effects ; Parkinson Disease/therapy ; Rats ; Rats, Sprague-Dawley ; Stem Cell Transplantation/methods ; Stem Cells/cytology ; Stem Cells/metabolism
    Chemical Substances Brain-Derived Neurotrophic Factor ; enhanced green fluorescent protein ; Green Fluorescent Proteins (147336-22-9) ; Oxidopamine (8HW4YBZ748)
    Language English
    Publishing date 2012
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1135816-6
    ISSN 1555-3892 ; 0963-6897
    ISSN (online) 1555-3892
    ISSN 0963-6897
    DOI 10.3727/096368911X586774
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: The Colayer Method as an Efficient Way to Genetically Modify Mesencephalic Progenitor Cells Transplanted into 6-OHDA Rat Model of Parkinson's Disease

    Andreas Ratzka / Ieva Kalve / Meltem Özer / André Nobre / Maike Wesemann / Julia Jungnickel / Christiane Köster-Patzlaff / Olga Baron / Claudia Grothe

    Cell Transplantation, Vol

    2012  Volume 21

    Abstract: Exogenous cell replacement represents a potent treatment option for Parkinson's disease. However, the low survival rate of transplanted dopaminergic neurons (DA) calls for methodological improvements. Here we evaluated a method to combine transient ... ...

    Abstract Exogenous cell replacement represents a potent treatment option for Parkinson's disease. However, the low survival rate of transplanted dopaminergic neurons (DA) calls for methodological improvements. Here we evaluated a method to combine transient genetic modification of neuronal progenitor cells with an optimized cell culture protocol prior to intrastriatal transplantation into 6-hydroxydopamine (6-OHDA) unilateral lesioned rats. Plasmid-based delivery of brain-derived neurotrophic factor (BDNF) increases the number of DA neurons, identified by tyrosine hydroxylase immunoreactivity (TH-ir), by 25% in vitro, compared to enhanced green fluorescence protein (EGFP)-transfected controls. However, the nucleofection itself, especially the cell detachment and reseeding procedure, decreases the TH-ir neuron number to 40% compared with nontransfected control cultures. To circumvent this drawback we established the colayer method, which contains a mix of nucleofected cells reseeded on top of an adherent sister culture in a ratio 1:3. In this setup TH-ir neuron number remains high and could be further increased by 25% after BDNF transfection. Comparison of both cell culture procedures (standard and colayer) after intrastriatal transplantation revealed a similar DA neuron survival as seen in vitro. Two weeks after grafting TH-ir neuron number was strongly reduced in animals receiving the standard EGFP-transfected cells (271 ± 62) compared to 1,723 ± 199 TH-ir neurons in the colayer group. In contrast to the in vitro results, no differences in the number of grafted TH-ir neurons were observed between BDNF, EGFP, and nontransfected colayer groups, neither 2 nor 13 weeks after transplantation. Likewise, amphetamine and apomorphine-induced rotational behavior improved similarly over time in all groups. Nevertheless, the colayer protocol provides an efficient way for neurotrophic factor release by transplanted progenitor cells and will help to study the effects of candidate factors on survival and integration of transplanted DA ...
    Keywords Medicine ; R
    Subject code 571
    Language English
    Publishing date 2012-04-01T00:00:00Z
    Publisher SAGE Publishing
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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