#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

-Induced Activation of EGFR Prevents Autophagy Protein-Mediated Killing of the Parasite


Toxoplasma gondii resides in an intracellular compartment (parasitophorous vacuole) that excludes transmembrane molecules required for endosome - lysosome recruitment. Thus, the parasite survives by avoiding lysosomal degradation. However, autophagy can re-route the parasitophorous vacuole to the lysosomes and cause parasite killing. This raises the possibility that T. gondii may deploy a strategy to prevent autophagic targeting to maintain the non-fusogenic nature of the vacuole. We report that T. gondii activated EGFR in endothelial cells, retinal pigment epithelial cells and microglia. Blockade of EGFR or its downstream molecule, Akt, caused targeting of the parasite by LC3+ structures, vacuole-lysosomal fusion, lysosomal degradation and killing of the parasite that were dependent on the autophagy proteins Atg7 and Beclin 1. Disassembly of GPCR or inhibition of metalloproteinases did not prevent EGFR-Akt activation. T. gondii micronemal proteins (MICs) containing EGF domains (EGF-MICs; MIC3 and MIC6) appeared to promote EGFR activation. Parasites defective in EGF-MICs (MIC1 ko, deficient in MIC1 and secretion of MIC6; MIC3 ko, deficient in MIC3; and MIC1-3 ko, deficient in MIC1, MIC3 and secretion of MIC6) caused impaired EGFR-Akt activation and recombinant EGF-MICs (MIC3 and MIC6) caused EGFR-Akt activation. In cells treated with autophagy stimulators (CD154, rapamycin) EGFR signaling inhibited LC3 accumulation around the parasite. Moreover, increased LC3 accumulation and parasite killing were noted in CD154-activated cells infected with MIC1-3 ko parasites. Finally, recombinant MIC3 and MIC6 inhibited parasite killing triggered by CD154 particularly against MIC1-3 ko parasites. Thus, our findings identified EGFR activation as a strategy used by T. gondii to maintain the non-fusogenic nature of the parasitophorous vacuole and suggest that EGF-MICs have a novel role in affecting signaling in host cells to promote parasite survival.


Vyšlo v časopise: -Induced Activation of EGFR Prevents Autophagy Protein-Mediated Killing of the Parasite. PLoS Pathog 9(12): e32767. doi:10.1371/journal.ppat.1003809
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003809

Souhrn

Toxoplasma gondii resides in an intracellular compartment (parasitophorous vacuole) that excludes transmembrane molecules required for endosome - lysosome recruitment. Thus, the parasite survives by avoiding lysosomal degradation. However, autophagy can re-route the parasitophorous vacuole to the lysosomes and cause parasite killing. This raises the possibility that T. gondii may deploy a strategy to prevent autophagic targeting to maintain the non-fusogenic nature of the vacuole. We report that T. gondii activated EGFR in endothelial cells, retinal pigment epithelial cells and microglia. Blockade of EGFR or its downstream molecule, Akt, caused targeting of the parasite by LC3+ structures, vacuole-lysosomal fusion, lysosomal degradation and killing of the parasite that were dependent on the autophagy proteins Atg7 and Beclin 1. Disassembly of GPCR or inhibition of metalloproteinases did not prevent EGFR-Akt activation. T. gondii micronemal proteins (MICs) containing EGF domains (EGF-MICs; MIC3 and MIC6) appeared to promote EGFR activation. Parasites defective in EGF-MICs (MIC1 ko, deficient in MIC1 and secretion of MIC6; MIC3 ko, deficient in MIC3; and MIC1-3 ko, deficient in MIC1, MIC3 and secretion of MIC6) caused impaired EGFR-Akt activation and recombinant EGF-MICs (MIC3 and MIC6) caused EGFR-Akt activation. In cells treated with autophagy stimulators (CD154, rapamycin) EGFR signaling inhibited LC3 accumulation around the parasite. Moreover, increased LC3 accumulation and parasite killing were noted in CD154-activated cells infected with MIC1-3 ko parasites. Finally, recombinant MIC3 and MIC6 inhibited parasite killing triggered by CD154 particularly against MIC1-3 ko parasites. Thus, our findings identified EGFR activation as a strategy used by T. gondii to maintain the non-fusogenic nature of the parasitophorous vacuole and suggest that EGF-MICs have a novel role in affecting signaling in host cells to promote parasite survival.


Zdroje

1. CarruthersVB, BoothroydJC (2007) Pulling together: an integrated model of Toxoplasma cell invasion. Curr Opin Microbiol 10: 83–89.

2. CarruthersVB, TomleyFM (2008) Receptor-ligand interaction and invasion: micronemeproteins in apicomplexans. Subcell Biochem 47: 33–45.

3. AnantharamanV, IyerLM, BalajiS, AravindL (2007) Adhesion molecules and other secreted host-interaction determinants in Apicomplexa: insights from comparative geneomics. Int Rev Cytol 262: 1–74.

4. TomleyFM, SoldatiDS (2001) Mix and match modules: structure and function of microneme proteins in apicomplexan parasites. Trends Parasitol 17: 81–88.

5. SibleyLD (2011) Invasion and intracellular survival by protozoan parasites. Immunol Rev 240: 72–91.

6. Soldati-FavreD (2008) Molecular dissection of host cell invasion by the apicomplexans: the glideosome. Parasite 15: 197–205.

7. BoothroydJC, DubremetzJF (2008) Kiss and spit: the dual roles of Toxoplasma rhoptries. Nat Rev Microbiol 6: 79–88.

8. BesteiroS, DubremetzJF, LebrunM (2011) The moving junction of apicomplexan parasites: a key structure for invasion. Cell Microbiol 13: 797–805.

9. MordueDG, DesaiN, DustinM, SibleyLD (1999) Invasion by Toxoplasma gondii establishes a moving junction that selectively excludes host cell plasma membrane proteins on the basis of their membrane anchoring. J Exp Med 190: 1783–1792.

10. MordueDG, HakanssonS, NiesmanI, SibleyLD (1999) Toxoplasma gondii resides in a vacuole that avoids fusion with host cell endocytic and exocytic vescicular pathways. Exp Parasitol 92: 87–99.

11. MartensS, ParvanovaI, ZerrahnJ, GriffithsG, SchellG, et al. (2005) Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases. PLoS Pathogens 1: 187–201.

12. ZhaoZ, FuxB, GoodwinM, DunayIR, StrongD, et al. (2008) Autophagosome-independent essential function for the autophagy protein Atg5 in cellular immunity to intracellular pathogens. Cell Host Microbe 4: 458–469.

13. AndradeRM, WessendarpM, GubbelsMJ, StriepenB, SubausteCS (2006) CD40 induces macrophage anti-Toxoplasma gondii activity by triggering autophagy-dependent fusion of pathogen-containing vacuoles and lysosomes. J Clin Invest 116: 2366–2377.

14. PortilloJ-AC, OkenkaG, ReedE, SubausteA, Van GrolJ, et al. (2010) The CD40-autophagy pathway is needed for host protection despite IFN-γ-dependent immunity and CD40 induces autophagy via control of p21 levels. Plos One 5: e14472.

15. Van GrolJ, Muniz-FelicianoL, PortilloJ-AC, BonilhaVL, SubausteCS (2013) CD40 induces anti-Toxoplasma gondii activity in non-hematopoietic cells dependent on autophagy proteins. Infect Immun 81: 2002–2011.

16. MizushimaN, YoshimoriT, OhsumiY (2010) The role of Atg proteins in autophagosome formation. Annu Rev Cell Dev Biol 27: 107–132.

17. LevineB, MizushimaN, VirginHW (2011) Autophagy in immunity and inflammation. Nature 469: 323–335.

18. OgawaM, YoshimoriT, SuzukiT, SagaraH, MizushimaN, et al. (2004) Escape of intracellular Shigella from autophagy. Science 307: 727–731.

19. TalloczyZ, VirginHW, LevineB (2006) PKR-dependent autophagic degradation of herpes simplex virus type 1. Autophagy 2: 24–29.

20. OrvedahlA, AlexanderD, TalloczyZ, SunQ, WeiY, et al. (2007) HSV-1 ICP34.5 confers neurovirulence by targeting the Beclin 1 autophagy protein. Cell Host & Microbe 1: 23–35.

21. YoshikawaY, OgawaM, HainT, YoshidaM, FukumatsuM, et al. (2009) Listeria monocytogenes ActA-mediated escape from autophagic recognition. Nat Cell Biol 11: 1233–1240.

22. EX, HwangS, OhS, LeeJ-S, JeongJH, et al. (2009) Viral Bcl-2-mediated evasion of autophagy aids chronic infection of gHerpesvirus 68. PLoS Pathog 5: e10000609.

23. KyeiGB, DinkinsC, DavisAS, RobertsE, SinghSB, et al. (2009) Autophagy pathway intersects with HIV-1 biosynthesis and regulates viral yields in macrophages. J Cell Biol 186: 255–268.

24. ChoyA, DancourtJ, MugoB, O'ConnorTJ, IsbergRR, et al. (2012) The Legionella effector RavZ inhibits host autophagy through irreversible Atg8 deconjugation. Science 338: 1072–1076.

25. BlanchetFP, MorisA, NikolicDS, LehmannM, CardinaudS, et al. (2010) Human immunodeficiency virus-1 inhibition of immunoamphisomes in dendritic cells impairs early innate and adaptive immune responses. Immunity 32: 654–669.

26. KumarDM, NathL, KamalMA, VarshneyA, JainA, et al. (2010) Genome-wide analysis of the host intracellular network that regulates survival of Mycobacterium tuberculosis. Cell 140: 731–743.

27. AlessiDR, AndjelkovicM, CaudwellB, CronP, MorriceN, et al. (1996) Mechanisms of activation of protein kinase B by insulin and IGF-1. EMBO J 15: 6541–6551.

28. ChanTO, RittenhouseSE, TsichlisPN (1999) AKT/PKB and other D3 phosphoinositide-regulated kinases: kinase actvation by phosphoinositide-dependent phosphorylation. Annu Rev Biochem 68: 965–1014.

29. StokoeD, StephensLR, CopelandT, GaffneyPRJ, ReeseCB, et al. (1997) Dual role of phosphatidylinositol-3,4,5-triphosphate in the activation of protein kinase B. Science 277: 567–570.

30. ServantG, WeinerOD, HerzmarkP, BallaT, SedatJW, et al. (2000) Polarization of chemoattractant receptor signaling during neutrophil chemtoaxis. Science 287: 1037–1040.

31. KimL, DenkersEY (2006) Toxoplasma gondii triggers Gi-dependent PI3-kinase signaling required for inhibition of host cell apoptosis. J Cell Sci 119: 2119–2126.

32. JoinerKA, FuhrmanSA, MietinnenH, KasperLH, MellmanI (1990) Toxoplasma gondii: fusion competence of parasitophorous vacuoles in Fc receptor transfected fibroblasts. Science 249: 641–646.

33. MordueDG, SibleyLD (1997) Intracellular fate of vacuoles containing Toxoplasma gondii is determined at the time of formation and depends on the mechanisms of entry. J Immunol 159: 4452–4459.

34. CoppensI, DunnJD, RomanoJD, PypaertM, ZhangH, et al. (2006) Toxoplasma gondii sequesters lysosomes from mammalian hosts in the vacuolar space. Cell 125: 261–274.

35. ScarlattiF, BauvyC, VentrutiA, SalaG, CluzeaudF, et al. (2004) Ceramide-mediated macroautophagy involves inhibition of protein kinase B and up-regulation of Beclin 1. J Biol Chem 279: 18384–18391.

36. HemmingsBA, RestucciaDF (2012) PI3K-PKB/Akt pathway. Cold Spring Harb Perspect Biol 4: a011189.

37. TigyiG, ParrillA (2003) Molecular mechanisms of lysophosphatidic acid action. Prog Lipid Res 42: 498–526.

38. CarruthersVB (2002) Host cell invasion by the opportunistic pathogen Toxoplasma gondii. Acta Tropica 81: 111–122.

39. CeredeO, DubremetzJF, SoeteM, DesleeD, VialH, et al. (2005) Synergistic role of micronemal proteins in Toxoplasma gondii virulence. J Exp Med 201: 453–463.

40. HuynhM-H, CarruthersVB (2006) Toxoplasma MIC2 is a major determinant of invasion and virulence. PLoS Pathogens 2: e84.

41. SheinerL, SantosJM, KlagesN, ParussiniF, JemmelyN, et al. (2010) Toxoplasma gondii transmembrane microneme proteins and their modular design. Mol Microbiol 77: 912–929.

42. MeissnerM, ReissM, ViebigN, CarruthersVB, TourselC, et al. (2002) A family of transmembrane microneme proteins of Toxoplasma gondii contain EGF-like domains and function as escorters. J Cell Sci 115: 563–574.

43. MoroL, DolceL, CabodiS, EB, Boeri ErbaE, et al. (2002) Integrin-induces epidermal growth factor (EGF) receptor activation requires c-Src and p130Cas and leads to phosphorylation of specific EGF receptor tyrosines. J Biol Chem 277: 9405–9414.

44. KrugAW, SchusterC, GassnerB, FreudingerR, MildenbergerS, et al. (2002) Human epidermal growth factor receptor-1 expression renders chinese hamster ovary cells sensitive to alternative aldosterone signaling. J Biol Chem 277.

45. YardenY, SliwkowskiMX (2001) Untangling the ErbB signalling network. Nat Rev Mol Cell Biol 2: 127–137.

46. ReissM, ViebigN, BrechtS, FourmauxMN, SoeteM, et al. (2001) Identification and characterization of an escorter for two secretory adhesins in Toxoplasma gondii. J Cell Biol 152: 563–578.

47. KesslerH, Hern-GotzA, HeggeS, RauchM, Soldati-FavreD, et al. (2008) Micronem protein 8 - a new essential invasion factor in Toxoplasma gondii. J Cell Sci 121: 947–956.

48. CeredeO, DubremetzJF, BoutD, LebrunM (2002) The Toxoplasma gondii protein MIC3 requires pro-peptide cleavage and dimerization to function as adhesin. EMBO J 21: 2526–2536.

49. Van Grol J, Subauste MC, Andrade RM, Fujinaga K, Nelson JA, et al.. (2010) HIV-1 inhibits autophagy in bystander macrophages/monocytic cells through Src-Akt and STAT3. PLoS One: e11733.

50. WangX, McCulloughKD, FrankeTF, HolbrookNJ (2000) Epidermal growth factor receptor-dependent Akt activation by oxidative stress enhances cell survival. J Biol Chem 275: 14624–14631.

51. MahajanK, MahajanNP (2012) PI3K-independent AKT activation in cancers: a treasure trove for novel therapeutics. J Cell Physiol 227: 3178–3184.

52. ZhouW, QuanJ-H, LeeY-H, ShinD-W, ChaG-H (2013) Toxoplasma gondii proliferation require down-regulation of host Nox4 expression via activation of PI3 kinase/Akt signaling pathway. Plos One 8: e66306.

53. SobolewskaA, GajewskaM, ZarzynskaJ, GajkowskaB, MotylT (2009) IGF-I, EGF, and sex steroids regulate autophagy in bovine mammary epithelial cells via the mTOR pathway. Eur J Cell Biol 88: 117–130.

54. MaynardAA, DvorakK, KhailovaL, DobrenenH, ArganbrightKM, et al. (2010) Epidermal growth factor reduces autophagy in intestinal epithelium and in the rat model of necrotizing enterocolitis. Am J Physiol Gastrointest Liver Physiol 299: G614–G622.

55. WangY, WeissLM, OrlofskyA (2009) Host cell autophagy is induced by Toxoplasma gondii and contributes to parasite growth. J Biol Chem 284: 1694–1701.

56. KoffJL, ShaoMXG, KimS, UekiIF, NadelJA (2006) Pseudomonas lipopolysaccharide accelerates wound repair via activation of a novel epithelial cell signaling cascade. J Immunol 177: 8693–8700.

57. KeatesS, SougioultzisS, KeatesAC, ZhaoD, PeekRMJ, et al. (2001) cag+ Helicobacter pylori induce transactivation of the epidermal growth factor receptor in AGS epithelial cells. J Biol Chem 276: 48127–48134.

58. FrankCG, ReguerloV, RotherM, MorantaD, MaeurerAP, et al. (2013) Klebsiella pneumoniae targets an EGF receptor-dependent pathway to subvert inflammation. Cell Microbiol 15: 1212–33.

59. KungC-P, MeckesDG, Raab-TraubN (2011) Epstein-Barr virus LMP1 activates EGFR, STAT3, and ERK through effects on PKCd. J Virol 85: 4399–4408.

60. MikamiF, GuH, JonoH, AndalabiA, KaiH, et al. (2005) Epidermal growth factor receptor acts as a negative regulator for bacterium nontypable Haemophilus influenzae-induced Toll-like receptor 2 expression via an Src-dependent p38 mitogen-activated protein kinase signaling pathway. J Biol Chem 280: 36185–36194.

61. EierhoffT, HrinciusER, RescherU, LudwigS, EhrhardtC (2010) The epidermal growth factor receptor (EGFR) promotes uptake of Influenza A viruses (IAV) into host cells. PLoS Pathog 6: e1001099.

62. ChhipaRR, WuY, IpC (2011) AMPK-mediated autophagy is a survival mechanism in androgen-dependent prostate cancer cells subjected to androgen deprivation and hypoxia. Cell Signal 23: 1466–1472.

63. O'FarrellF, WangS, KathederN, RustenTE, SamkovlisC (2013) Two-tiered control of epithelial growth and autophagy by the insulin receptor and the Ret-like receptor, Stitcher. PLoS Biol 11: e1001612.

64. BoothroydJC, DubremetzJF (2008) Kiss and spit: the dual roles of Toxoplasma rhoptries. Nat Rev Microbiol 6: 79–88.

65. LaliberteJ, CarruthersVB (2008) Host cell manipulation by the human pathogen Toxoplasma gondii. Cell Mol Life Sci 65: 1900–1915.

66. LengJ, ButcherBA, DenkersEY (2009) Dysregulation of macrophage signal transduction by Toxoplasma gondii: past progress and recent advances. Parasite Immunol 31: 717–728.

67. PollardAM, KnollLJ, MordueDG (2009) The role of specific Toxoplasma gondii molecules in manipulation of innate immunity. Trends Parasitol 25: 491–494.

68. AndradeRM, PortilloJ-AC, WessendarpM, SubausteCS (2005) CD40 signaling in macrophages induces anti-microbial activity against an intracellular pathogen independently of IFN-γ and reactive nitrogen intermediates. Infect Immun 73: 3115–3123.

69. GubbelsMJ, LiC, StriepenB (2003) High-throughput growth assay for Toxoplasma gondii using yellow fluorescent protein. Antimicrob Agents Chemother 47: 309–316.

70. RoosDS, DonaldRG, MorrissetteNS, MoultonAL (1994) Molecular tools for genetic dissection of the protozoan parasite Toxoplasma gondii. Methods Cell Biol 45: 27–63.

71. KafsackBFC, BeckersCJ, CarruthersVB (2004) Synchronous invasion of host cells by Toxoplasma gondii. Mol Biochem Parasitol 136: 309–311.

72. BajorathJ, SeyamaK, NonoyamaS, OchsHD, AruffoA (1996) Classification of mutations in the human CD40 ligand, gp39, that are associated with X-linked hyper IgM syndrome. Protein Sci 5: 531–534.

73. PortilloJ-AC, Van GrolJ, ZhengL, OkenkaG, GentilK, et al. (2008) CD40 mediates retinal inflammation and neuro-vascular degeneration. J Immunol 181: 8719–8726.

74. LiuB, SawmynadenK, MarchantJ, SimpsonP, MatthewsS (2009) Complete resonance assigments for the MIC2 associated protein from Toxoplasma gondii. Biomol NMR Assign 3: 81–83.

75. SaourosS, Edwards-JonesB, ReissM, SawmynadenK, CotaE, et al. (2005) A novel galectin-like domain from Toxoplasma gondii micronemal protein 1 assists the folding, assembly, and transport of a cell adhesion complex. J Biol Chem 280: 38583–38591.

76. KwonY, HofmannT, MontellC (2007) Integration of phosphoinositide- and calmodulin-mediated regulation of TRPC6. Mol Cell 25: 491–503.

77. MengQ, XiaC, FangJ, RojanasakulY, JiangB-H (2006) Role of PI3K and AKT specific isoforms in ovarian cancer cell migration, invasion and proliferation through the p70S6K1 pathway. Cell Signal 18: 2262–2271.

78. KuoPL, HsuYL, ChoCY (2006) Plumbagin induces G2-M arrest and autophagy by inhibiting the Akt/mammalian target of rapamycin pathway in breast cancer cells. Mol Cancer Ther 5: 3209–3221.

79. YuL, AlvaA, SuH, DuttP, FreundtE, et al. (2004) Regulation of an ATG7-beclin 1 program of autophagic cell death by caspase-8. Science 304: 1500–1502.

80. HirataY, OhmaeT, ShibataW, MaedaS, OguraK, et al. (2006) MyD88 and TNF Receptor-Assocaited Factor 6 are critical signal transducers in Helicobacter pylori-infected human epithelial cells. J Immunol 176: 3796–3803.

81. KangC-S, ZhangZ-Y, JiaZ-F, WangG-X, QiuM-Z, et al. (2006) Suppression of EGFR expression by antisense or small interference RNA inhibits U251 glioma cell growth in vitro and in vivo. Cancer Gene Ther 13: 530–538.

82. KimS-E, ChoiK-Y (2007) EGF receptor is involved in WNT3a-mediated proliferation and motility of NIH3T3 cells via ERK pathway activation. Cellular Signaling 19: 1554–1564.

83. FujiokaH, TandlerB, ConsoloMC, KarnikP (2013) Division of mitochondria in cultured human fibroblasts. Microsc Res Tech [Epub ahead of print].

Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

Článok vyšiel v časopise

PLOS Pathogens


2013 Číslo 12
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#