Metal arsenic mediated enhancement of type-2 immunity in brains with altered locomotive activities in mice with autism-like behavioral characteristics |
Han, Ha‑Jung
(College of Bio and Medical Sciences, Department of Occupational Health, Daegu Catholic University)
Lee, JaeHee (College of Bio and Medical Sciences, Department of Occupational Health, Daegu Catholic University) Lim, GyeongDong (College of Bio and Medical Sciences, Department of Occupational Health, Daegu Catholic University) Park, JungEun (College of Bio and Medical Sciences, Department of Occupational Health, Daegu Catholic University) Gautam, Ravi (College of Bio and Medical Sciences, Department of Occupational Health, Daegu Catholic University) Jo, JiHun (College of Bio and Medical Sciences, Department of Occupational Health, Daegu Catholic University) Kim, ChangYul (Graduate School Department of Toxicology, Daegu Catholic University) Heo, Yong (College of Bio and Medical Sciences, Department of Occupational Health, Daegu Catholic University) |
1 | Vahidnia A, van der Voet GB, de Wolf FA (2007) Arsenic neurotoxicity-a review. Hum Exp Toxicol 26:823-832. https://doi.org/10.1177/0960327107084539 DOI |
2 | Kern JK, Geier DA, Homme KG et al (2017) Developmental neurotoxicants and the vulnerable male brain: a systemic review of suspected neurotoxicants that disproportionally afect male. Acta Neurobiol Exp 77:269-296. https://doi.org/10.21307/ane-2017-061 DOI |
3 | IACC (Interagency Autism Coordinating Committee) (2020) 2019 IACC Summary of Advances in Autism Spectrum Disorder Research. U.S. Department of Health and Human Services Interagency Autism Coordinating Committee. National Institute of Health, Bethesda. https://iacc.hhs.gov/publications/summaryof-advances/2019/ |
4 | Jin X, Wang M, Shentu J et al (2020) Inhibition of acetylcholinesterase activity and β-amyloid oligomer formation by 6-bromotrypatamine A, a multi-target anti-Alzheimer's molecule. Oncol Lett 19:1593-1601. https://doi.org/10.3892/ol.2019.11226 DOI |
5 | Nadler JJ, Moy SS, Dold G et al (2004) Automated apparatus for quantitation of social approach behaviors in mice. Genes Brain Behav 3:303-314. https://doi.org/10.1111/j.1601-183X.2004.00071.x DOI |
6 | Lo S-C, Scearce-Levie K, Sheng M (2016) Characterization of social behaviors in caspase-3 defcient mice. Sci Rep 6:18335. https://doi.org/10.1038/srep18335 DOI |
7 | Heo Y, Parsons PJ, Lawrence DA (1996) Lead diferentially modifes cytokine production in vitro and in vivo. Toxicol Appl Phamacol 138:149-157. https://doi.org/10.1006/taap.1996.0108 DOI |
8 | Rahman A, Islam MS, Tony SR et al (2021) T helper 2-driven immune dysfunction in chronic arsenic-exposed individuals and its link to the features of allergic asthma. Toxicol Appl Pharmacol 420:115532. https://doi.org/10.1016/j.taap.2021.115532 DOI |
9 | Ye Y, Gaugler B, Mohty M et al (2020) Old dog, new trick: Trivalent arsenic as an immunomodulatory drug. Br J Pharmacol 177:2199-2214. https://doi.org/10.1111/bph.15011 DOI |
10 | VanDenBerg KR, Freeborn RA, Liu S et al (2017) Inhibition of early T cell cytokine production by arsenic trioxide occurs independently of Nrf2. PLoS ONE 6:e0185579. https://doi.org/10.1371/journal.pone.0185579 DOI |
11 | Molloy CA, Morrow AL, Meinzen-Derr J et al (2006) Elevated cytokine levels in children with autism spectrum disorder. J Neuroimmunol 172:198-205. https://doi.org/10.1016/j.neuroim.2005.11.007 DOI |
12 | Gladysz D, Krzywdzinska A, Hozyasz KK (2018) Immune abnormalities in autism spectrum disorder-could they hold promise for causative treatment? Mol Neurobiol 55:6387-6435. https://doi.org/10.1007/s12035-017-0822-x DOI |
13 | Firacative C, Gressler AE, Schubert K et al (2018) Identifcation of T helper (Th)1- and Th2-associated antigens of Cryptococcus neoformans in a murine model of pulmonary infection. Sci Rep 8:2681. https://doi.org/10.1038/s41598-018-21039-z DOI |
14 | Hessabi M, Rahbar MH, Dobrescu I et al (2019) Concentration of lead, mercury, arsenic, cadmium, manganese, and aluminium in blood of Romanian children suspected of having autism spectrum disorder. Int J Environ Res Public Health 16:2303. https://doi.org/10.3390/ijerph16132303 DOI |
15 | Stigler KA, Sweeten TL, Posey DJ, McDougle CJ (2009) Autism and immune factors: a comprehensive review. Res Autsim Spectr Disord 3:840-860. https://doi.org/10.1016/j.rasd.2009.01.007 DOI |
16 | Faraji J, Karimi M, Lawrence C et al (2018) Non-diagnostic symptoms in a mouse model of autism in relation to neuroanatomy: the BTBR strain reinvestigated. Transl Psychiatry 8:234. https://doi.org/10.1038/s41398-018-0280-x DOI |
17 | Jasien JM, Daimon CM, Wang R et al (2014) The efects of aging on the BTBR mouse model of autism spectrum disorder. Front Aging Neurosci 6:225. https://doi.org/10.3389/fnagi.2014.00225 DOI |
18 | Moy SS, Nadler JJ, Young NB et al (2007) Mouse behavioral tasks relevant to autism: phenotypes of ten inbred strains. Behav Brain Res 176:4-20. https://doi.org/10.1016/j.bbr.2006.07.030 DOI |
19 | Modabbernia A, Velthorst E, Reichenberg A (2017) Environmental risk factors for autism: an evidence based review of systematic reviews and meta-analyses. Mol Autism 8:13. https://doi.org/10.1186/s13229-017-0121-4 DOI |
20 | Li H, Li H, Li Y, Liu Y, Zhao Z (2018) Blood mercury, arsenic, cadmium, and lead in children with autism spectrum disorder. Biol Trace Elem Res 181:31-37. https://doi.org/10.1007/s12011-017-1002-6 DOI |
21 | Zheng W, Aschner M, Ghersi-Egea J-F (2003) Brain barrier systems: a new frontier in metal neurotoxicological research. Toxicol Appl Pharmacol 192:1-11. https://doi.org/10.1016/s0041-008x(03)00251-5 DOI |
22 | Rahbar MH, Samms-Vaughan M, Lee M-J et al (2020) Interaction between a mixture of heavy metals (lead, mercury, arsenic, cadmium, manganese, aluminium) and GSTP1, GSTT1, and GSTM1 in relation to autism spectrum disorder. Res Autism Spectr Disord 79:101681. https://doi.org/10.1016/j.rasd.2020.101681 DOI |
23 | Heo Y, Zhang Y, Gao D, Miller VM, Lawrence DA (2011) Aberrant immune responses in a mouse with behavioral disorders. PLoS ONE 6:e20912. https://doi.org/10.1371/journal.pone.0020912 DOI |
24 | Hwang S-R, Kim C-Y, Shin K-M, Jo J-H, Kim H-A, Heo Y (2015) Altered expression levels of neurodevelopmental proteins in fetal brains of BTBR T+tf/J mice with autism-like behavioral characteristics. J Toxicol Environ Health Part A 78:516-523. https://doi.org/10.1080/15287394.2015.1010466 DOI |
25 | Kim S-N, Jo G-H, Kim H-A, Heo Y (2016) Aberrant IgG isotype generation in mice with abnormal behaviors. J Immunotoxicol 13:92-96. https://doi.org/10.3109/1547691X.2015.1014581 DOI |
26 | Kern JK, Geier DA, Sykes LK, Haley BE, Geier MR (2016) The relationship between mercury and autism: a comprehensive review and discussion. J Trace Elem Med Biol 37:8-24. https://doi.org/10.1016/j.jtemb.2016.06.002 DOI |
27 | Edmiston E, Ashwood P, van de Water J (2017) Autoimmunity, autoantibodies, and autism spectrum disorders. Biol Psychiatry 81:383-390. https://doi.org/10.1016/j.biopsych.2016.08.031 DOI |
28 | Yang M, Silverman JL, Crawley JN (2011) Automated three-chambered social approach task for mice, Chap. 8. In: Gerfen CR, Giniger E, Holmes A, Wray S, Kurt M (ed) Current protocols in neuroscience. Wiley, Hoboken, Unit 8.26. https://doi.org/10.1002/0471142301.ns082s56 DOI |
29 | Fiore M, Barone R, Copat C et al (2020) Metal and essential element levels in hair and association with autism severity. J Trace Elem Med Biol 57:99-103. https://doi.org/10.1016/j.jtemb.2019.126409 DOI |
30 | Wang M, Hossain F, Sulaiman R, Ren X (2019) Exposure to inorganic arsenic and lead and autism spectrum disorder in children: a systemic review and meta-analysis. Chem Res Toxicol 32:1904-1919. https://doi.org/10.1021/acs.chemrestox.9b00134 DOI |
31 | Holson JF, Stump DG, Clevidence KJ, Knapp JF, Farr CH (2000) Evaluation of the prenatal developmental toxicity of orally administered arsenic trioxide in rats. Food Chem Toxicol 38:459-466. https://doi.org/10.1016/s0278-6915(00)00015-6 DOI |
32 | Chang C-Y, Guo H-R, Tsai W-C et al (2015) Subchronic arsenic exposure induces anxiety-like behaviors in normal mice and enhances depression-like behaviors in the chemically induced mouse model of depression. Biomed Res Int 2015:159015. https://doi.org/10.1155/2015/159015 DOI |
33 | Chao OY, Yunger R, Yang Y-M (2018) Behavioral assessment of BTBR T+Itpr3tf/J mice by tests of object attention and elevated open platform: implications for an animal model of psychiatric comorbidity in autism. Behav Brain Res 347:140-147. https://doi.org/10.1016/j.bbr.2018.03.014 DOI |
34 | Biswas R, Ghosh P, Banerjee N et al (2008) Analysis of T cell proliferation and cytokine secretion in the individuals exposed to arsenic. Hum Exp Toxicol 27:381-386. https://doi.org/10.1177/09600327108094607 DOI |
35 | Dickerson AS, Rahbar MH, Bakian AV et al (2016) Autism spectrum disorder prevalence and associations with air concentrations of lead, mercury, and arsenic. Environ Monit Assess 188:407. https://doi.org/10.1007/s10661-016-5405-1 DOI |
36 | Mesiano G, Zini R, Montagner G et al (2017) Analytical and dynamic secretory profle of patient-derived cytokine-induced killer cells. Mol Med 23:235-246. https://doi.org/10.2119/molmed.2017.00084 DOI |