Microglia and Alzheimer's disease.

Microglia play a major role in the cellular response associated with the pathological lesions of Alzheimer's disease. As brain-resident macrophages, microglia elaborate and operate under several guises that seem reminiscent of circulating and tissue monocytes of the leucocyte repertoire. Although microglia bear the capacity to synthesize amyloid beta, current evidence is most consistent with their phagocytic role. This largely involves the removal of cerebral amyloid and possibly the transformation of amyloid beta into fibrils. The phagocytic functions also encompass the generation of cytokines, reactive oxygen and nitrogen species, and various proteolytic enzymes, events that may exacerbate neuronal damage rather than incite outgrowth or repair mechanisms. Microglia do not appear to function as true antigen-presenting cells. However, there is circumstantial evidence that suggests functional heterogeneity within microglia. Pharmacological agents that suppress microglial activation or reduce microglial-mediated oxidative damage may prove useful strategies to slow the progression of Alzheimer's disease.

[1]  P. Gottschall β‐amyloid induction of gelatinase B secretion in cultured microglia: inhibition by dexamethasone and indomethacin , 1996, Neuroreport.

[2]  K. Brunden,et al.  β-Amyloid induces increased release of interleukin-1β from lipopolysaccharide-activated human monocytes , 1996, Journal of Neuroimmunology.

[3]  D. Kooy,et al.  Separate blood and brain origins of proliferating cells during gliosis in adult brains , 1990, Brain Research.

[4]  D. Walker,et al.  Activation of Macrophages by Alzheimer β Amyloid Peptide , 1994 .

[5]  N. Peress,et al.  Differential Expression of TGF-β1, 2 and 3 Isotypes in Alzheimer's Disease: A Comparative Immunohistochemical Study with Cerebral Infarction, Aged Human and Mouse Control Brains , 1995, Journal of neuropathology and experimental neurology.

[6]  Douglas Walker,et al.  Inflammation and Alzheimer's disease pathogenesis , 1996, Neurobiology of Aging.

[7]  L. Haverkamp,et al.  Senile plaques stimulate microglia to release a neurotoxin found in Alzheimer brain , 1995, Neurochemistry International.

[8]  B. Hyman,et al.  Expression of the Very Low‐Density Lipoprotein Receptor (VLDL‐r), an Apolipoprotein‐E Receptor, in the Central Nervous System and in Alzheimer's Disease , 1996, Journal of neuropathology and experimental neurology.

[9]  G. Kreutzberg Microglia: a sensor for pathological events in the CNS , 1996, Trends in Neurosciences.

[10]  P. Mcgeer,et al.  The inflammatory response system of brain: implications for therapy of Alzheimer and other neurodegenerative diseases , 1995, Brain Research Reviews.

[11]  J. Loike,et al.  Scavenger receptor-mediated adhesion of microglia to β-amyloid fibrils , 1996, Nature.

[12]  T. Miyakawa,et al.  Identification of monocyte chemoattractant protein‐1 in senile plaques and reactive microglia of Alzheimer's disease , 1997, Psychiatry and clinical neurosciences.

[13]  S. Pierce,et al.  A case for chaperones in antigen processing. , 1992, Immunology today.

[14]  K. Dyke The possible role of peroxynitrite in Alzheimer's disease: a simple hypothesis that could be tested more thoroughly , 1997 .

[15]  W. Jefferies,et al.  Reactive microglia specifically associated with amyloid plaques in Alzheimer's disease brain tissue express melanotransferrin , 1996, Brain Research.

[16]  H. Akiyama,et al.  Activated microglial cells are colocalized with perivascular deposits of amyloid-beta protein in Alzheimer's disease brain. , 1997, Stroke.

[17]  C. Masters,et al.  Extracellular Matrix Influences the Biogenesis of Amyloid Precursor Protein in Microglial Cells (*) , 1995, The Journal of Biological Chemistry.

[18]  R. Veerhuis,et al.  The role of complement and activated microglia in the pathogenesis of Alzheimer's disease , 1996, Neurobiology of Aging.

[19]  D. Ferrari,et al.  Activation of microglial cells by β-amyloid protein and interferon-γ , 1995, Nature.

[20]  T. Iwatsubo,et al.  Association of A beta 40-positive senile plaques with microglial cells in the brains of patients with Alzheimer's disease and in non-demented aged individuals. , 1996, Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration.

[21]  P. Gottschall,et al.  Regulation of matrix metalloproteinase expressions in astrocytes, microglia and neurons. , 1996, Neuroimmunomodulation.

[22]  C. Cotman,et al.  Bax Protein Expression Is Increased in Alzheimer's Brain: Correlations with DNA Damage, Bcl‐2 Expression, and Brain Pathology , 1997, Journal of neuropathology and experimental neurology.

[23]  V. Perry,et al.  OVERRIDING THE BRAIN'S INTRINSIC RESISTANCE TO LEUKOCYTE RECRUITMENT WITH INTRAPARENCHYMAL INJECTIONS OF RECOMBINANT CHEMOKINES , 1996, Neuroscience.

[24]  R. Nelson,et al.  Anti‐inflammatory action of dapsone: inhibition of neutrophil adherence is associated with inhibition of chemoattractant‐induced signal transduction , 1997, Journal of leukocyte biology.

[25]  S. Younkin,et al.  Amyloid β protein (Aβ) removal by neuroglial cells in culture , 1995, Neurobiology of Aging.

[26]  X. Chen,et al.  RAGE and amyloid-β peptide neurotoxicity in Alzheimer's disease , 1996, Nature.

[27]  B. Seed,et al.  Expression of the CD6 T lymphocyte differentiation antigen in normal human brain , 1990, Journal of Neuroimmunology.

[28]  D. Munoz,et al.  Role of microglia in senile plaque formation , 1995, Neurobiology of Aging.

[29]  A. Dahlström,et al.  Microglial in neurodegenerative disorders: emphasis on Alzheimer's disease. , 1997, Gerontology.

[30]  M. Emmerling,et al.  Morphology and Toxicity of Aβ-(1-42) Dimer Derived from Neuritic and Vascular Amyloid Deposits of Alzheimer's Disease* , 1996, The Journal of Biological Chemistry.

[31]  M. Sporn,et al.  Inducible nitric oxide synthase in tangle-bearing neurons of patients with Alzheimer's disease , 1996, The Journal of experimental medicine.

[32]  Sidney Strickland,et al.  Excitotoxin-induced neuronal degeneration and seizure are mediated by tissue plasminogen activator , 1995, Nature.

[33]  C. Colton,et al.  Modulation of nitric oxide production in human macrophages by apolipoprotein-E and amyloid-beta peptide. , 1997, Biochemical and biophysical research communications.

[34]  N L Foster,et al.  PET of peripheral benzodiazepine binding sites in the microgliosis of Alzheimer's disease. , 1995, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[35]  H. Yamaguchi,et al.  Microglial activation in early stages of amyloid β protein deposition , 1997, Acta Neuropathologica.

[36]  W. Griffin,et al.  Glial‐Neuronal Interactions in Alzheimer's Disease: The Potential Role of a ‘Cytokine Cycle’ in Disease Progression , 1998, Brain pathology.

[37]  K. Beyreuther,et al.  Bcl‐xl‐Specific antibody labels activated microglia associated with Alzheimer's disease and other pathological states , 1997, Journal of neuroscience research.

[38]  K. Barron The microglial cell. A historical review , 1995, Journal of the Neurological Sciences.

[39]  E. Uemura,et al.  Integrin Mac-1 and β-amyloid in microglial release of nitric oxide , 1997, Brain Research.

[40]  F. Rossi,et al.  Activation of nuclear factor-κB by β-amyloid peptides and interferon-γ in murine microglia , 1997, Journal of Neuroimmunology.

[41]  A. Mantovani,et al.  Beta-amyloid (25-35) peptide and IFN-gamma synergistically induce the production of the chemotactic cytokine MCP-1/JE in monocytes and microglial cells. , 1996, Journal of immunology.

[42]  F. Maxfield,et al.  Microglial Cells Internalize Aggregates of the Alzheimer's Disease Amyloid β-Protein Via a Scavenger Receptor , 1996, Neuron.

[43]  J. Sedgwick,et al.  Microglia induce CD4 T lymphocyte final effector function and death , 1996, The Journal of experimental medicine.

[44]  B. Hyman,et al.  Immunohistochemical localization of tissue factor pathway inhibitor-1 (TFPI-1), a Kunitz proteinase inhibitor, in Alzheimer's disease , 1996, Brain Research.

[45]  Douglas R. McDonald,et al.  β-Amyloid Fibrils Activate Parallel Mitogen-Activated Protein Kinase Pathways in Microglia and THP1 Monocytes , 1998, The Journal of Neuroscience.

[46]  C. Masters,et al.  In‐vitro matured human macrophages express Alzheimer's βA4‐amyloid precursor protein indicating synthesis in microglial cells , 1991, FEBS letters.

[47]  D. Walker,et al.  Interaction of Alzheimer β-amyloid peptide with the human monocytic cell line THP-1 results in a protein kinase C-dependent secretion of tumor necrosis factor-α , 1997, Brain Research.

[48]  Brian J Cummings,et al.  Localization and Cell Association of C1q in Alzheimer's Disease Brain , 1996, Experimental Neurology.

[49]  A. Planas,et al.  Transforming growth factor-α (TGF-α) and epidermal growth factor-receptor (EGF-R) immunoreactivity in normal and pathologic brain , 1996, Progress in Neurobiology.

[50]  D. Butterfield,et al.  Brain Regional Correspondence Between Alzheimer's Disease Histopathology and Biomarkers of Protein Oxidation , 1995, Journal of neurochemistry.

[51]  G. Kreutzberg,et al.  Inflammatory reaction in experimental autoimmune encephalomyelitis (EAE) is accompanied by a microglial expression of the βA4‐amyloid precursor protein (APP) , 1995, Glia.

[52]  H. Lassmann,et al.  Bone marrow derived elements and resident microglia in brain inflammation , 1993, Glia.

[53]  P. Gebicke-haerter,et al.  Cyclooxygenase‐2 expression in rat microglia is induced by adenosine A2a‐receptors , 1996, Glia.

[54]  A. Roher,et al.  Specific Domains of β-Amyloid from Alzheimer Plaque Elicit Neuron Killing in Human Microglia , 1996, The Journal of Neuroscience.

[55]  D. Walker,et al.  Expression of CD43 in human microglia and its downregulation in Alzheimer's disease , 1996, Journal of Neuroimmunology.

[56]  G. Bing,et al.  Selective killing of cholinergic neurons by microglial activation in basal forebrain mixed neuronal/glial cultures. , 1995, Biochemical and biophysical research communications.

[57]  T. Morgan,et al.  Age-Related Activation of Microglia and Astrocytes: In Vitro Studies Show Persistent Phenotypes of Aging, Increased Proliferation, and Resistance to Down-Regulation , 1998, Neurobiology of Aging.

[58]  R. Mrak,et al.  Neuritic plaque evolution in Alzheimer’s disease is accompanied by transition of activated microglia from primed to enlarged to phagocytic forms , 1997, Acta Neuropathologica.

[59]  P. Mcgeer,et al.  Granules in glial cells of patients with Alzheimer's disease are immunopositive for C-terminal sequences of β-amyloid protein , 1996, Neuroscience Letters.

[60]  G. Forloni,et al.  β-AMYLOID FRAGMENT POTENTIATES IL-6 AND TNF-α SECRETION BY LPS IN ASTROCYTES BUT NOT IN MICROGLIA , 1997 .

[61]  G. Murphy,et al.  β-Amyloid Peptide Secretion by a Microglial Cell Line Is Induced by β-Amyloid-(25–35) and Lipopolysaccharide* , 1996, The Journal of Biological Chemistry.

[62]  R. Veerhuis,et al.  Amyloid β Protein Primes Cultured Rat Microglial Cells for an Enhanced Phorbol 12‐Myristate 13‐Acetate‐Induced Respiratory Burst Activity , 1996, Journal of neurochemistry.

[63]  L. Lue,et al.  Characterization of glial cultures from rapid autopsies of Alzheimer's and control patients , 1996, Neurobiology of Aging.

[64]  C. Cotman,et al.  Cultured Rat Microglia Express C1q and Receptor for C1q: Implications for Amyloid Effects on Microglia , 1995, Experimental Neurology.

[65]  T. Yamada,et al.  Microglial localization of α-interferon receptor in human brain tissues , 1995, Neuroscience Letters.

[66]  Masanori Kato,et al.  Immunohistochemical detection of coagulation factor XIIIa in postmortem human brain tissue , 1995, Neuroscience Letters.

[67]  Y. Ichimori,et al.  β-Amyloid protein-dependent nitric oxide production from microglial cells and neurotoxicity , 1996, Brain Research.

[68]  Steven A. Johnson,et al.  Inability to Detect β-Amyloid Protein Precursor mRNA in Alzheimer Plaque-Associated Microglia , 1993, Experimental Neurology.

[69]  R. Simone,et al.  The Costimulatory Molecule B7 is Expressed on Human Microglia in Culture and in Multiple Sclerosis Acute Lesions , 1995, Journal of neuropathology and experimental neurology.

[70]  M. Freeman,et al.  Expression of the macrophage scavenger receptor, a multifunctional lipoprotein receptor, in microglia associated with senile plaques in Alzheimer's disease. , 1996, The American journal of pathology.

[71]  T. Morgan,et al.  Astrocytes and Microglia Respond to Estrogen with Increased apoE mRNAin Vivoandin Vitro , 1997, Experimental Neurology.

[72]  C. Hulette,et al.  Microglia Are Not Exclusively Associated with Plaque‐rich Regions of the Dentate Gyms in Alzheimer's Disease , 1996, Journal of neuropathology and experimental neurology.

[73]  T Suenaga,et al.  Alterations of the blood-brain barrier and glial cells in white-matter lesions in cerebrovascular and Alzheimer's disease patients. , 1996, Stroke.

[74]  W. Streit,et al.  The brain's immune system. , 1995, Scientific American.

[75]  J. Abkowitz,et al.  Kinetics of central nervous system microglial and macrophage engraftment: analysis using a transgenic bone marrow transplantation model. , 1997, Blood.

[76]  G. Cole,et al.  Scavenging of Alzheimer's amyloid β‐protein by microglia in culture , 1996, Journal of neuroscience research.

[77]  R. Xue,et al.  Amyloid Precursor Protein Metabolism in Primary Cell Cultures of Neurons, Astrocytes, and Microglia , 1996, Journal of neurochemistry.

[78]  R. Kalaria The Immunopathology of Alzheimer's Disease and Some Related Disorders , 1993, Brain pathology.

[79]  D. Premkumar,et al.  Cellular aspects of the inflammatory response in Alzheimer's disease. , 1996, Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration.

[80]  E. Uemura,et al.  Microglial release of nitric oxide by the synergistic action of β-amyloid and IFN-γ , 1995, Brain Research.

[81]  D. Lorton β-Amyloid-induced IL-1β release from an activated human monocyte cell line is calcium- and G-protein-dependent , 1997, Mechanisms of Ageing and Development.

[82]  A. LeBlanc,et al.  Processing of Amyloid Precursor Protein in Human Primary Neuron and Astrocyte Cultures , 1997, Journal of neurochemistry.

[83]  S. Barger,et al.  Microglial activation by Alzheimer amyloid precursor protein and modulation by apolipoprotein E , 1997, Nature.

[84]  M. Mckinney,et al.  Topographic associations between DNA fragmentation and Alzheimer's disease neuropathology in the hippocampus , 1997, Neurochemistry International.

[85]  C. Duyckaerts,et al.  ApoE immunoreactivity and microglial cells in Alzheimer's disease brain , 1995, Neuroscience Letters.

[86]  G. Perry,et al.  Amyloid P component and other acute-phase proteins associated with cerebellar Aβ-deposits in Alzheimer's disease , 1993, Brain Research.

[87]  C. Kufta,et al.  Adult human glial cells can present target antigens to HLA-restricted cytotoxic T-cells , 1990, Journal of Neuroimmunology.

[88]  Douglas R. McDonald,et al.  Amyloid Fibrils Activate Tyrosine Kinase-Dependent Signaling and Superoxide Production in Microglia , 1997, The Journal of Neuroscience.

[89]  J. Wegiel,et al.  Review: David Oppenheimer Memorial Lecture 1995: Some neuropathological aspects of Alzheimer's disease and its relevance to other disciplines * , 1996, Neuropathology and applied neurobiology.

[90]  S. Ferroni,et al.  Support of Homeostatic Glial Cell Signaling: A Novel Therapeutic Approach by Propentofylline a , 1997, Annals of the New York Academy of Sciences.

[91]  D. Walker,et al.  Localization of perlecan (or a perlecan‐related macromolecule) to isolated microglia in vitro and to microglia/macrophages following infusion of beta‐amyloid protein into rodent hippocampus , 1997, Glia.

[92]  L. Mucke,et al.  Cellular signaling roles of TGFβ, TNFα and βAPP in brain injury responses and Alzheimer's disease , 1997, Brain Research Reviews.

[93]  F. Maxfield,et al.  Slow Degradation of Aggregates of the Alzheimer’s Disease Amyloid β-Protein by Microglial Cells* , 1997, The Journal of Biological Chemistry.