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  1. Article ; Online: The role of aging and brain-derived neurotrophic factor signaling in expression of base excision repair genes in the human brain.

    Lautrup, Sofie / Myrup Holst, Camilla / Yde, Anne / Asmussen, Stine / Thinggaard, Vibeke / Larsen, Knud / Laursen, Lisbeth Schmidt / Richner, Mette / Vaegter, Christian B / Prieto, G Aleph / Berchtold, Nicole / Cotman, Carl W / Stevnsner, Tinna

    Aging cell

    2023  Volume 22, Issue 9, Page(s) e13905

    Abstract: DNA damage is a central contributor to the aging process. In the brain, a major threat to the DNA is the considerable amount of reactive oxygen species produced, which can inflict oxidative DNA damage. This type of damage is removed by the base excision ... ...

    Abstract DNA damage is a central contributor to the aging process. In the brain, a major threat to the DNA is the considerable amount of reactive oxygen species produced, which can inflict oxidative DNA damage. This type of damage is removed by the base excision repair (BER) pathway, an essential DNA repair mechanism, which contributes to genome stability in the brain. Despite the crucial role of the BER pathway, insights into how this pathway is affected by aging in the human brain and the underlying regulatory mechanisms are very limited. By microarray analysis of four cortical brain regions from humans aged 20-99 years (n = 57), we show that the expression of core BER genes is largely downregulated during aging across brain regions. Moreover, we find that expression of many BER genes correlates positively with the expression of the neurotrophin brain-derived neurotrophic factor (BDNF) in the human brain. In line with this, we identify binding sites for the BDNF-activated transcription factor, cyclic-AMP response element-binding protein (CREB), in the promoter of most BER genes and confirm the ability of BDNF to regulate several BER genes by BDNF treatment of mouse primary hippocampal neurons. Together, these findings uncover the transcriptional landscape of BER genes during aging of the brain and suggest BDNF as an important regulator of BER in the human brain.
    MeSH term(s) Animals ; Humans ; Mice ; Aging/genetics ; Aging/metabolism ; Brain/metabolism ; Brain-Derived Neurotrophic Factor/genetics ; Brain-Derived Neurotrophic Factor/metabolism ; DNA Repair/genetics ; Signal Transduction/genetics
    Chemical Substances Brain-Derived Neurotrophic Factor ; BDNF protein, human (7171WSG8A2)
    Language English
    Publishing date 2023-06-19
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2113083-8
    ISSN 1474-9726 ; 1474-9718
    ISSN (online) 1474-9726
    ISSN 1474-9718
    DOI 10.1111/acel.13905
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: An integrin-contactin complex regulates CNS myelination by differential Fyn phosphorylation.

    Laursen, Lisbeth Schmidt / Chan, Colin W / ffrench-Constant, Charles

    The Journal of neuroscience : the official journal of the Society for Neuroscience

    2009  Volume 29, Issue 29, Page(s) 9174–9185

    Abstract: The understanding of how adhesion molecules mediate the axon-glial interactions in the CNS that ensure target-dependent survival of oligodendrocytes and initiate myelination remains incomplete. Here, we investigate how signals from adhesion molecules can ...

    Abstract The understanding of how adhesion molecules mediate the axon-glial interactions in the CNS that ensure target-dependent survival of oligodendrocytes and initiate myelination remains incomplete. Here, we investigate how signals from adhesion molecules can be integrated to regulate these initial steps of myelination. We first demonstrate that the Ig superfamily molecule contactin is associated in oligodendrocytes with integrins, extracellular matrix receptors that regulate target-dependent survival by amplification of growth factor signaling. This amplification is inhibited by small interfering RNA-mediated knockdown of contactin in oligodendrocytes. In contrast, the presence of L1-Fc, the extracellular portion of a contactin ligand expressed on axons, enhanced survival and additionally promoted myelination in cocultures of neurons and oligodendrocytes. We further demonstrate that the signals from contactin and integrin are integrated by differential phosphorylation of the Src family kinase Fyn. Integrin induced dephosphorylation of the inhibitory Tyr-531, whereas contactin increased phosphorylation of both Tyr-531 and the activating Tyr-420. The combined effect is an enhanced activity of Fyn and also a dynamic regulation of the phosphorylation/dephosphorylation balance of Fyn, as required for normal cell adhesion and spreading. We conclude, therefore, that a novel integrin/contactin complex coordinates signals from extracellular matrix and the axonal surface to regulate both oligodendrocyte survival and myelination by controlling Fyn activity.
    MeSH term(s) Animals ; Axons/physiology ; Cell Adhesion Molecules, Neuronal/metabolism ; Cell Survival/physiology ; Cells, Cultured ; Coculture Techniques ; Contactins ; Extracellular Matrix/metabolism ; Gene Knockdown Techniques ; Integrin alpha6beta1/metabolism ; Integrins/metabolism ; Models, Neurological ; Myelin Sheath/physiology ; Neurons/physiology ; Oligodendroglia/physiology ; Phosphorylation ; Proto-Oncogene Proteins c-fyn/metabolism ; RNA, Small Interfering/metabolism ; Rats ; Tyrosine/metabolism
    Chemical Substances Cell Adhesion Molecules, Neuronal ; Contactins ; Integrin alpha6beta1 ; Integrins ; RNA, Small Interfering ; Tyrosine (42HK56048U) ; Fyn protein, rat (EC 2.7.10.2) ; Proto-Oncogene Proteins c-fyn (EC 2.7.10.2)
    Language English
    Publishing date 2009-07-22
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 604637-x
    ISSN 1529-2401 ; 0270-6474
    ISSN (online) 1529-2401
    ISSN 0270-6474
    DOI 10.1523/JNEUROSCI.5942-08.2009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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