Exosomes, mitochondrial DNA and microglia: the fateful triangle in autism

 

Autism Spectrum Disorder (ASD) remains without distinct pathogenesis and effective treatment. Extracellular vesicles (EVs or exosomes) are secreted in blood or other biological fluids by diverse cell types.

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EVs are generated either from the cell when multivesicular bodies (MVBs) fuse with the plasma membranes or they are released directly from the plasma membrane.3 EVs can be isolated from serum, plasma, urine and other biological fluids and have been shown to contain RNA, DNA, lipids or proteins that are delivered to the surrounding cells or carried to distal sites.

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EVs have been implicated in brain disorders,

3

,

4

,

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but their presence in ASD has not been investigated.

We isolated EVs from children with ASD (n=20, 4-12 years old), and total EV-associated protein was increased as compared (P<0.022) to age and sex-matched normotypic controls (n=10). Moreover, EVs isolated from serum of patients with ASD stimulated cultured human microglia to secrete (184.3 ± 7.62 pg/mL, p<0.0001) the pro-inflammatory cytokine interleukin IL-1β.

The source or cargo of the EVs isolated from the serum of children with ASD is not presently known.  Exosomes could come from peripheral immune cells, such as mast cells,

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and could cross the blood-brain-barrier.

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Alternatively, astrocytes and glioblastoma cells

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were reported to secrete exosomes containing mitochondrial DNA (mtDNA). We showed that mast cells secrete mtDNA, some of which is inside exosomes,

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and we further reported that mtDNA is increased in the serum of children with ASD.

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Extracellular mtDNA would act a an “innate pathogen” and trigger a stong auto-inflammatory response.

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Given that food allergies,

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asthma

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and atopic dermatitis,

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,

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which involve mast cells,

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have been associated with ASD, EVs could also contain known mast cell-derived microglia triggers such histamine and tryptase

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or neurotensin.

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They could even contain autoantibodies against brain epitopes.

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 These findings suggest a possible link between EVs and inflammation of the brain and indicate a novel pathogenetic mechanism that may also be used for objective diagnosis, or targeted for the treatment of ASD.

(Funded by an Anonymus grant to TCT)

 

Reference List

 

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      2.   Chen X, Liang H, Zhang J, Zen K, Zhang CY. Horizontal transfer of microRNAs: molecular mechanisms and clinical applications. Protein Cell 2012; 3(1):28-37.

      3.   Tsilioni I, Panagiotidou S, Theoharides TC. Exosomes in neurologic and psychiatric disorders. Clin Ther 2014; 36(6):882-888.

      4.   Kawikova I, Askenase PW. Diagnostic and therapeutic potentials of exosomes in CNS diseases. Brain Res 2014; 1617:63-71.

      5.   Turpin D, Truchetet ME, Faustin B et al. Role of extracellular vesicles in autoimmune diseases. Autoimmun Rev 2016; 15(2):174-183.

      6.   Skokos D, Le PS, Villa I et al. Mast cell-dependent B and T lymphocyte activation is mediated by the secretion of immunologically active exosomes. J Immunol 2001; 166(2):868-876.

      7.   Chen CC, Liu L, Ma F et al. Elucidation of exosome migration across the Blood-Brain Barrier model in vitro. Cell Mol Bioeng 2016; 9(4):509-529.

      8.   Guescini M, Genedani S, Stocchi V, Agnati LF. Astrocytes and glioblastoma cells release exosomes carrying mtDNA. J Neural Transm 2010; 117(1):1-4.

      9.   Zhang B, Asadi S, Weng Z, Sismanopoulos N, Theoharides TC. Stimulated human mast cells secrete mitochondrial components that have autocrine and paracrine inflammatory actions. PloS One 2012; 7(12):e49767.

    10.   Zhang B, Angelidou A, Alysandratos KD et al. Mitochondrial DNA and anti-mitochondrial antibodies in serum of autistic children. J Neuroinflammation 2010; 7(1):80.

    11.   Theoharides TC, Asadi S, Panagiotidou S, Weng Z. The "missing link" in autoimmunity and autism: Extracellular mitochondrial components secreted from activated live mast cells. Autoimmun Rev 2013; 12(12):1136-1142.

    12.   Lyall K, Van de WJ, Ashwood P, Hertz-Picciotto I. Asthma and allergies in children with Autism Spectrum Disorders: Results from the CHARGE Study. Autism Res 2015; 8(5):567-574.

    13.   Kotey S, Ertel K, Whitcomb B. Co-occurrence of autism and asthma in a nationally-representative sample of children in the United States. J Autism Dev Disord 2014; 44(12):3083-3088.

    14.   Liao TC, Lien YT, Wang S, Huang SL, Chen CY. Comorbidity of atopic disorders with Autism Spectrum Disorder and Attention Deficit/Hyperactivity Disorder. J Pediatr 2016; 171:248-255.

    15.   Billeci L, Tonacci A, Tartarisco G, Ruta L, Pioggia G, Gangemi S. Association between atopic dermatitis and Autism Spectrum Disorders: A systematic review. Am J Clin Dermatol 2015; 16(5):371-388.

    16.   Theoharides TC, Valent P, Akin C. Mast Cells, mastocytosis, and related disorders. N Engl J Med 2015; 373(2):163-172.

    17.   Theoharides TC., Tsilioni I, Patel AB, Doyle R. Atopic diseases and inflammation of the brain in the pathogenesis of autism spectrum disorders. Transl Psychiatry 2016; 6(6):e844.

    18.   Patel AB, Tsilioni I, Leeman SE, Theoharides TC. Neurotensin stimulates sortilin and mTOR in human microglia inhibitable by methoxyluteolin, a potential therapeutic target for autism. Proc Natl Acad Sci U S A 2016; 113:E7049-E7058.

    19.   Rossi CC, Van de WJ, Rogers SJ, Amaral DG. Detection of plasma autoantibodies to brain tissue in young children with and without autism spectrum disorders. Brain Behav Immun 2011; 25(6):1123-1135.

 

 

 

Theoharis C. Theoharides, MS, MPhil, PhD, MD

Theoharis C. Theoharides, MS, MPhil, PhD, MD, FAAAAI, is Professor of Pharmacology and Internal Medicine and the Director of Molecular Immunopharmacology and Drug Discovery, Department of  Immunology, at Tufts University School of Medicine.