Secreted miR-34a in astrocytic shedding vesicles enhanced the vulnerability of dopaminergic neurons to neurotoxins by targeting Bcl-2

Susu Mao, Qi Sun, Hui Xiao, Chenyu Zhang, Liang Li

PDF(1520 KB)
PDF(1520 KB)
Protein Cell ›› 2015, Vol. 6 ›› Issue (7) : 529-540. DOI: 10.1007/s13238-015-0168-y
RESEARCH ARTICLE
RESEARCH ARTICLE

Secreted miR-34a in astrocytic shedding vesicles enhanced the vulnerability of dopaminergic neurons to neurotoxins by targeting Bcl-2

Author information +
History +

Abstract

MicroRNAs (miRNAs) are a class of noncoding RNAs that regulates target gene expression at posttranscriptional level, leading to further biological functions. We have demonstrated that microvesicles (MVs) can deliver miRNAs into target cells as a novel way of intercellular communication. It is reported that in central nervous system, glial cells release MVs, which modulate neuronal function in normal condition. To elucidate the potential role of glial MVs in disease, we evaluated the effects of secreted astrocytic MVs on stress condition. Our results demonstrated that after Lipopolysaccharide (LPS) stimulation, astrocytes released shedding vesicles (SVs) that enhanced vulnerability of dopaminergic neurons to neurotoxin. Further investigation showed that increased astrocytic miR-34a in SVs was involved in this progress via targeting anti-apoptotic protein Bcl-2 in dopaminergic neurons. We also found that inhibition of astrocytic miR-34a after LPS stimulation can postpone dopaminergic neuron loss under neurotoxin stress. These data revealed a novel mechanism underlying astrocyte-neuron interaction in disease.

Keywords

astrocyte / shedding vesicles / miR-34a / dopaminergic neurons / Bcl-2

Cite this article

Download citation ▾
Susu Mao, Qi Sun, Hui Xiao, Chenyu Zhang, Liang Li. Secreted miR-34a in astrocytic shedding vesicles enhanced the vulnerability of dopaminergic neurons to neurotoxins by targeting Bcl-2. Protein Cell, 2015, 6(7): 529‒540 https://doi.org/10.1007/s13238-015-0168-y

References

[1]
Al-Nedawi K, Meehan B, Rak J (2009) Microvesicles: messengers and mediators of tumor progression. Cell cycle8: 2014-2018
CrossRef Google scholar
[2]
Antonucci F, Turola E, Riganti L, Caleo M, Gabrielli M, Perrotta C, Novellino L, Clementi E, Giussani P, Viani P (2012) Microvesicles released from microglia stimulate synaptic activity via enhanced sphingolipid metabolism. EMBO J31: 1231-1240
CrossRef Google scholar
[3]
Barbagallo D, Piro S, Condorelli AG, Mascali LG, Urbano F, Parrinello N, Monello A, Statello L, Ragusa M, Rabuazzo AM (2013) miR-296-3p, miR-298-5p and their downstream networks are causally involved in the higher resistance of mammalian pancreatic alpha cells to cytokine-induced apoptosis as compared to beta cells. Bmc Genomics14: 62
CrossRef Google scholar
[4]
Bianco F, Perrotta C, Novellino L, Francolini M, Riganti L, Menna E, Saglietti L, Schuchman EH, Furlan R, Clementi E (2009) Acid sphingomyelinase activity triggers microparticle release from glial cells. EMBO J28: 1043-1054
CrossRef Google scholar
[5]
Chen Y, Vartiainen NE, Ying W, Chan PH, Koistinaho J, Swanson RA (2001) Astrocytes protect neurons from nitric oxide toxicity by a glutathione-dependent mechanism. J Neurochem77: 1601-1610
CrossRef Google scholar
[6]
Forno LS, DeLanney LE, Irwin I, Di Monte D, Langston JW (1992) Astrocytes and Parkinson’s disease. Prog Brain Res94: 429-436
CrossRef Google scholar
[7]
Furman JL, Norris CM (2014) Calcineurin and glial signaling: neuroinflammation and beyond. J Neuroinflamm11: 158
CrossRef Google scholar
[8]
Gundersen HJ, Bagger P, Bendtsen TF, Evans SM, Korbo L, Marcussen N, Moller A, Nielsen K, Nyengaard JR, Pakkenberg B (1988) The new stereological tools: disector, fractionator, nucleator and point sampled intercepts and their use in pathological research and diagnosis. APMIS96: 857-881
CrossRef Google scholar
[9]
Gupta A, Pulliam L (2014) Exosomes as mediators of neuroinflammation. J Neuroinflamm11: 68
CrossRef Google scholar
[10]
Hirsch EC, Hunot S, Damier P, Brugg B, Faucheux BA, Michel PP, Ruberg M, Muriel MP, Mouatt-Prigent A, Agid Y (1999) Glial cell participation in the degeneration of dopaminergic neurons in Parkinson’s disease. Adv Neurol80: 9-18
[11]
Hockenbery DM, Oltvai ZN, Yin XM, Milliman CL, Korsmeyer SJ (1993) Bcl-2 functions in an antioxidant pathway to prevent apoptosis. Cell75: 241-251
CrossRef Google scholar
[12]
Hu G, Yao H, Chaudhuri AD, Duan M, Yelamanchili SV, Wen H, Cheney PD, Fox HS, Buch S (2012) Exosome-mediated shuttling of microRNA-29 regulates HIV Tat and morphine-mediated neuronal dysfunction. Cell death Dis3: e381
CrossRef Google scholar
[13]
Janowska-Wieczorek A, Wysoczynski M, Kijowski J, Marquez-Curtis L, Machalinski B, Ratajczak J, Ratajczak MZ (2005) Microvesicles derived from activated platelets induce metastasis and angiogenesis in lung cancer. Int J Cancer113: 752-760
CrossRef Google scholar
[14]
Jung HJ, Suh Y (2014) Circulating miRNAs in ageing and ageingrelated diseases. J Genet Genomics41: 465-472
CrossRef Google scholar
[15]
Keller S, Sanderson MP, Stoeck A, Altevogt P (2006) Exosomes: from biogenesis and secretion to biological function. Immunol Lett107: 102-108
CrossRef Google scholar
[16]
Lee KW, Im JY, Woo JM, Grosso H, Kim YS, Cristovao AC, Sonsalla PK, Schuster DS, Jalbut MM, Fernandez JR (2013) Neuroprotective and anti-inflammatory properties of a coffee component in the MPTP model of Parkinson’s disease. Neurotherapeutics10: 143-153
CrossRef Google scholar
[17]
Lei SL, Zhao H, Yao HL, Chen Y, Lei ZD, Liu KJ, Yang Q (2014) Regulatory roles of microRNA-708 and microRNA-31 in proliferation, apoptosis and invasion of colorectal cancer cells. Oncol Lett8: 1768-1774
CrossRef Google scholar
[18]
Li XZ, Bai LM, Yang YP, Luo WF, Hu WD, Chen JP, Mao CJ, Liu CF (2009) Effects of IL-6 secreted from astrocytes on the survival of dopaminergic neurons in lipopolysaccharide-induced inflammation. Neurosci Res65: 252-258
CrossRef Google scholar
[19]
Liu C, Zhou CF, Gao F, Cai SY, Zhang C, Zhao LQ, Zhao F, Cao F, Lin J, Yang YY (2011) MiR-34a in Age and Tissue Related Radio-Sensitivity and Serum miR-34a as a Novel Indicator of Radiation Injury. Int J Biol Sci7: 221-233
CrossRef Google scholar
[20]
Liu Y, Zhao L, Li D, Yin Y, Zhang CY, Li J, Zhang Y (2013) Microvesicle-delivery miR-150 promotes tumorigenesis by upregulating VEGF, and the neutralization of miR-150 attenuate tumor development. Protein Cell4: 932-941
CrossRef Google scholar
[21]
Malavolta M, Basso A, Piacenza F, Costarelli L, Giacconi R, Mocchegiani E (2013) Peripheral mononuclear cell rejuvenation for senescence surveillance in Alzheimer disease. Curr Pharm Des19: 1720-1726
[22]
Morel O, Toti F, Hugel B, Freyssinet JM (2004) Cellular microparticles: a disseminated storage pool of bioactive vascular effectors. Curr Opin Hematol11: 156-164
CrossRef Google scholar
[23]
Niranjan R, Nath C, Shukla R (2010) The mechanism of action of MPTP-induced neuroinflammation and its modulation by melatonin in rat astrocytoma cells, C6. Free Radical Res44: 1304-1316
CrossRef Google scholar
[24]
Oeckl P, Lattke M, Wirth T, Baumann B, Ferger B (2012) Astrocytespecific IKK2 activation in mice is sufficient to induce neuroinflammation but does not increase susceptibility to MPTP. Neurobiol Dis48: 481-487
CrossRef Google scholar
[25]
Saijo K, Winner B, Carson CT, Collier JG, Boyer L, Rosenfeld MG, Gage FH, Glass CK (2009) A Nurr1/CoREST pathway in microglia and astrocytes protects dopaminergic neurons from inflammation-induced death. Cell137: 47-59
CrossRef Google scholar
[26]
Saura J, Pares M, Bove J, Pezzi S, Alberch J, Marin C, Tolosa E, Marti MJ (2003) Intranigral infusion of interleukin-1beta activates astrocytes and protects from subsequent 6-hydroxydopamine neurotoxicity. J Neurochem85: 651-661
CrossRef Google scholar
[27]
Scherr M, Elder A, Battmer K, Barzan D, Bomken S, Ricke-Hoch M, Schroder A, Venturini L, Blair HJ, Vormoor J (2014) Differential expression of miR-17∼92 identifies BCL2 as a therapeutic target in BCR-ABL-positive B-lineage acute lymphoblastic leukemia. Leukemia28: 554-565
CrossRef Google scholar
[28]
Shantsila E, Kamphuisen PW, Lip GY (2010) Circulating microparticles in cardiovascular disease: implications for atherogenesis and atherothrombosis. J Thromb Haemost8: 2358-2368
CrossRef Google scholar
[29]
Song T, Zhang X, Zhang L, Dong J, Cai W, Gao JP, Hong BF (2013) miR-708 promotes the development of bladder carcinoma via direct repression of Caspase-2. J Cancer Res Clin139: 1189-1198
CrossRef Google scholar
[30]
Stromberg I, Bjorklund H, Dahl D, Jonsson G, Sundstrom E, Olson L (1986) Astrocyte responses to dopaminergic denervations by 6-hydroxydopamine and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine as evidenced by glial fibrillary acidic protein immunohistochemistry. Brain Res Bull17: 225-236
CrossRef Google scholar
[31]
Sun L, Wu Z, Shao Y, Pu Y, Miu W, Yao J, Wu Y, Yang Z (2012) MicroRNA-34a suppresses cell proliferation and induces apoptosis inU87glioma stem cells. Technol CancerResTreat11: 483-490
[32]
Vlassov AV, Magdaleno S, Setterquist R, Conrad R (2012) Exosomes: current knowledge of their composition, biological functions, and diagnostic and therapeutic potentials. Biochim Biophysica Acta1820: 940-948
CrossRef Google scholar
[33]
Wang X, Liu P, Zhu H, Xu Y, Ma C, Dai X, Huang L, Liu Y, Zhang L, Qin C (2009) miR-34a, a microRNA up-regulated in a double transgenic mouse model of Alzheimer’s disease, inhibits bcl2 translation. Brain Res Bull80: 268-273
CrossRef Google scholar
[34]
Yang J, Liu X, Bhalla K, Kim CN, Ibrado AM, Cai J, Peng TI, Jones DP, Wang X (1997) Prevention of apoptosis by Bcl-2: release of cytochrome c from mitochondria blocked. Science275: 1129-1132
CrossRef Google scholar
[35]
Zhang Y, Liu D, Chen X, Li J, Li L, Bian Z, Sun F, Lu J, Yin Y, Cai X (2010) Secreted monocytic miR-150 enhances targeted endothelial cell migration. Molecular cell39: 133-144
CrossRef Google scholar
[36]
Zhou Y, Xiong M, Niu J, Sun Q, Su W, Zen K, Dai C, Yang J (2014) Secreted fibroblast-derived miR-34a induces tubular cell apoptosis in fibrotic kidney. J Cell Science127: 4494-4506
CrossRef Google scholar
[37]
Zhu H, Fan GC (2011) Extracellular/circulating microRNAs and their potential role in cardiovascular disease. Am J Cardiovasc Dis1: 138-149
[38]
Zomer A, Vendrig T, Hopmans ES, van Eijndhoven M, Middeldorp JM, Pegtel DM (2010) Exosomes: Fit to deliver small RNA. Communicative Integr Biol3: 447-450

RIGHTS & PERMISSIONS

2014 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
AI Summary AI Mindmap
PDF(1520 KB)

Accesses

Citations

Detail

Sections
Recommended

/