Placental Syncytium Forms a Biophysical Barrier against Pathogen Invasion
Fetal syncytiotrophoblasts form a unique fused multinuclear surface that is bathed in maternal blood, and constitutes the main interface between fetus and mother. Syncytiotrophoblasts are exposed to pathogens circulating in maternal blood, and appear to have unique resistance mechanisms against microbial invasion. These are due in part to the lack of intercellular junctions and their receptors, the Achilles heel of polarized mononuclear epithelia. However, the syncytium is immune to receptor-independent invasion as well, suggesting additional general defense mechanisms against infection. The difficulty of maintaining and manipulating primary human syncytiotrophoblasts in culture makes it challenging to investigate the cellular and molecular basis of host defenses in this unique tissue. Here we present a novel system to study placental pathogenesis using murine trophoblast stem cells (mTSC) that can be differentiated into syncytiotrophoblasts and recapitulate human placental syncytium. Consistent with previous results in primary human organ cultures, murine syncytiotrophoblasts were found to be resistant to infection with Listeria monocytogenes via direct invasion and cell-to-cell spread. Atomic force microscopy of murine syncytiotrophoblasts demonstrated that these cells have a greater elastic modulus than mononuclear trophoblasts. Disruption of the unusually dense actin structure – a diffuse meshwork of microfilaments - with Cytochalasin D led to a decrease in its elastic modulus by 25%. This correlated with a small but significant increase in invasion of L. monocytogenes into murine and human syncytium. These results suggest that the syncytial actin cytoskeleton may form a general barrier against pathogen entry in humans and mice. Moreover, murine TSCs are a genetically tractable model system for the investigation of specific pathways in syncytial host defenses.
Vyšlo v časopise:
Placental Syncytium Forms a Biophysical Barrier against Pathogen Invasion. PLoS Pathog 9(12): e32767. doi:10.1371/journal.ppat.1003821
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.ppat.1003821
Souhrn
Fetal syncytiotrophoblasts form a unique fused multinuclear surface that is bathed in maternal blood, and constitutes the main interface between fetus and mother. Syncytiotrophoblasts are exposed to pathogens circulating in maternal blood, and appear to have unique resistance mechanisms against microbial invasion. These are due in part to the lack of intercellular junctions and their receptors, the Achilles heel of polarized mononuclear epithelia. However, the syncytium is immune to receptor-independent invasion as well, suggesting additional general defense mechanisms against infection. The difficulty of maintaining and manipulating primary human syncytiotrophoblasts in culture makes it challenging to investigate the cellular and molecular basis of host defenses in this unique tissue. Here we present a novel system to study placental pathogenesis using murine trophoblast stem cells (mTSC) that can be differentiated into syncytiotrophoblasts and recapitulate human placental syncytium. Consistent with previous results in primary human organ cultures, murine syncytiotrophoblasts were found to be resistant to infection with Listeria monocytogenes via direct invasion and cell-to-cell spread. Atomic force microscopy of murine syncytiotrophoblasts demonstrated that these cells have a greater elastic modulus than mononuclear trophoblasts. Disruption of the unusually dense actin structure – a diffuse meshwork of microfilaments - with Cytochalasin D led to a decrease in its elastic modulus by 25%. This correlated with a small but significant increase in invasion of L. monocytogenes into murine and human syncytium. These results suggest that the syncytial actin cytoskeleton may form a general barrier against pathogen entry in humans and mice. Moreover, murine TSCs are a genetically tractable model system for the investigation of specific pathways in syncytial host defenses.
Zdroje
1. GoldenbergRL, HauthJC, AndrewsWW (2000) Intrauterine infection and preterm delivery. N Engl J Med 342: 1500–1507.
2. BeckS, WojdylaD, SayL, BetranAP, MerialdiM, et al. (2010) The worldwide incidence of preterm birth: a systematic review of maternal mortality and morbidity. Bull World Health Organ 88: 31–38.
3. RobbinsJR, BakardjievAI (2012) Pathogens and the placental fortress. Curr Opin Microbiol 15: 36–43.
4. PouillotR, HoelzerK, JacksonKA, HenaoOL, SilkBJ (2012) Relative risk of listeriosis in Foodborne Diseases Active Surveillance Network (FoodNet) sites according to age, pregnancy, and ethnicity. Clin Infect Dis 54 (Suppl 5) S405–410.
5. Vital signs: Listeria illnesses, deaths, and outbreaks–United States, 2009-2011. MMWR Morb Mortal Wkly Rep 62: 448–452.
6. MylonakisE, PaliouM, HohmannEL, CalderwoodSB, WingEJ (2002) Listeriosis during pregnancy: a case series and review of 222 cases. Medicine (Baltimore) 81: 260–269.
7. Siegman-IgraY, LevinR, WeinbergerM, GolanY, SchwartzD, et al. (2002) Listeria monocytogenes infection in Israel and review of cases worldwide. Emerg Infect Dis 8: 305–310.
8. BenshushanA, TsafrirA, ArbelR, RahavG, ArielI, et al. (2002) Listeria infection during pregnancy: a 10 year experience. Isr Med Assoc J 4: 776–780.
9. GellinBG, BroomeCV, BibbWF, WeaverRE, GaventaS, et al. (1991) The epidemiology of listeriosis in the United States–1986. Listeriosis Study Group. Am J Epidemiol 133: 392–401.
10. SchuchatA, LizanoC, BroomeCV, SwaminathanB, KimC, et al. (1991) Outbreak of neonatal listeriosis associated with mineral oil. Pediatr Infect Dis J 10: 183–189.
11. NotermansS, DufrenneJ, TeunisP, ChackrabortyT (1998) Studies on the risk assessment of Listeria monocytogenes. J Food Prot 61: 244–248.
12. ChaJ, BartosA, EgashiraM, HaraguchiH, Saito-FujitaT, et al. (2013) Combinatory approaches prevent preterm birth profoundly exacerbated by gene-environment interactions. J Clin Invest 123: 4063–4075.
13. ErlebacherA (2013) Immunology of the Maternal-Fetal Interface. Annu Rev Immunol
14. ZeldovichVB, BakardjievAI (2012) Host defense and tolerance: unique challenges in the placenta. PLoS Pathog 8: e1002804.
15. MedawarPB (1953) Some immunological and endocrinological problems raised by the evolution of viviparity in vertebrates. Symp Soc Exp Biol 7: 320–338.
16. MorG, CardenasI, AbrahamsV, GullerS (2011) Inflammation and pregnancy: the role of the immune system at the implantation site. Ann N Y Acad Sci 1221: 80–87.
17. Delorme-AxfordE, DonkerRB, MouilletJF, ChuT, BayerA, et al. (2013) Human placental trophoblasts confer viral resistance to recipient cells. Proc Natl Acad Sci U S A 110: 12048–12053.
18. MaltepeE, BakardjievAI, FisherSJ (2010) The placenta: transcriptional, epigenetic, and physiological integration during development. J Clin Invest 120: 1016–1025.
19. Benirschke K, Kaufmann P, Baergen RN (2006) Pathology of the Human Placenta.
20. RobbinsJR, SkrzypczynskaKM, ZeldovichVB, KapidzicM, BakardjievAI (2010) Placental syncytiotrophoblast constitutes a major barrier to vertical transmission of Listeria monocytogenes. PLoS Pathog 6: e1000732.
21. RobbinsJR, ZeldovichVB, PoukchanskiA, BoothroydJC, BakardjievAI (2012) Tissue barriers of the human placenta to infection with Toxoplasma gondii. Infect Immun 80: 418–428.
22. KoiH, ZhangJ, MakrigiannakisA, GetsiosS, MacCalmanCD, et al. (2002) Syncytiotrophoblast is a barrier to maternal-fetal transmission of herpes simplex virus. Biol Reprod 67: 1572–1579.
23. AplinJD, JonesCJ, HarrisLK (2009) Adhesion molecules in human trophoblast - a review. I. Villous trophoblast. Placenta 30: 293–298.
24. BonazziM, CossartP (2011) Impenetrable barriers or entry portals? The role of cell-cell adhesion during infection. J Cell Biol 195: 349–358.
25. OcklefordCD, WakelyJ, BadleyRA (1981) Morphogenesis of human placental chorionic villi: cytoskeletal, syncytioskeletal and extracellular matrix proteins. Proc R Soc Lond B Biol Sci 212: 305–316.
26. ChoiHJ, SandersTA, TormosKV, AmeriK, TsaiJD, et al. (2013) ECM-Dependent HIF Induction Directs Trophoblast Stem Cell Fate via LIMK1-Mediated Cytoskeletal Rearrangement. PLoS One 8: e56949.
27. TanakaS, KunathT, HadjantonakisAK, NagyA, RossantJ (1998) Promotion of trophoblast stem cell proliferation by FGF4. Science 282: 2072–2075.
28. BishopDK, HinrichsDJ (1987) Adoptive transfer of immunity to Listeria monocytogenes. The influence of in vitro stimulation on lymphocyte subset requirements. J Immunol 139: 2005–2009.
29. LecuitM, NelsonDM, SmithSD, KhunH, HuerreM, et al. (2004) Targeting and crossing of the human maternofetal barrier by Listeria monocytogenes: role of internalin interaction with trophoblast E-cadherin. Proc Natl Acad Sci U S A 101: 6152–6157.
30. BakardjievAI, StacyBA, FisherSJ, PortnoyDA (2004) Listeriosis in the pregnant guinea pig: a model of vertical transmission. Infect Immun 72: 489–497.
31. LecuitM, DramsiS, GottardiC, Fedor-ChaikenM, GumbinerB, et al. (1999) A single amino acid in E-cadherin responsible for host specificity towards the human pathogen Listeria monocytogenes. EMBO J 18: 3956–3963.
32. WollertT, PascheB, RochonM, DeppenmeierS, van den HeuvelJ, et al. (2007) Extending the host range of Listeria monocytogenes by rational protein design. Cell 129: 891–902.
33. BehmRJ, HoslerW, RitterE, BinningG (1986) Correlation between domain boundaries and surface steps: A scanning-tunneling-microscopy study on reconstructed Pt(100). Phys Rev Lett 56: 228–231.
34. HammerickKE, HuangZ, SunN, LamMT, PrinzFB, et al. (2011) Elastic properties of induced pluripotent stem cells. Tissue Eng Part A 17: 495–502.
35. SampathP, PollardTD (1991) Effects of cytochalasin, phalloidin, and pH on the elongation of actin filaments. Biochemistry 30: 1973–1980.
36. NagayamaK, NaganoY, SatoM, MatsumotoT (2006) Effect of actin filament distribution on tensile properties of smooth muscle cells obtained from rat thoracic aortas. J Biomech 39: 293–301.
37. Moreno-FloresS, BenitezR, VivancoM, Toca-HerreraJL (2010) Stress relaxation and creep on living cells with the atomic force microscope: a means to calculate elastic moduli and viscosities of cell components. Nanotechnology 21: 445101.
38. WakatsukiT, SchwabB, ThompsonNC, ElsonEL (2001) Effects of cytochalasin D and latrunculin B on mechanical properties of cells. J Cell Sci 114: 1025–1036.
39. RotschC, RadmacherM (2000) Drug-induced changes of cytoskeletal structure and mechanics in fibroblasts: an atomic force microscopy study. Biophys J 78: 520–535.
40. DrevetsDA, JelinekTA, FreitagNE (2001) Listeria monocytogenes-infected phagocytes can initiate central nervous system infection in mice. Infect Immun 69: 1344–1350.
41. BakardjievAI, TheriotJA, PortnoyDA (2006) Listeria monocytogenes traffics from maternal organs to the placenta and back. PLoS Pathog 2: e66.
42. MonackDM, TheriotJA (2001) Actin-based motility is sufficient for bacterial membrane protrusion formation and host cell uptake. Cell Microbiol 3: 633–647.
43. RobbinsJR, BarthAI, MarquisH, de HostosEL, NelsonWJ, et al. (1999) Listeria monocytogenes exploits normal host cell processes to spread from cell to cell. J Cell Biol 146: 1333–1350.
44. TilneyLG, PortnoyDA (1989) Actin filaments and the growth, movement, and spread of the intracellular bacterial parasite, Listeria monocytogenes. J Cell Biol 109: 1597–1608.
45. BerrymanM, GaryR, BretscherA (1995) Ezrin oligomers are major cytoskeletal components of placental microvilli: a proposal for their involvement in cortical morphogenesis. J Cell Biol 131: 1231–1242.
46. KingBF (1983) The organization of actin filaments in human placental villi. J Ultrastruct Res 85: 320–328.
47. NansA, MohandasN, StokesDL (2011) Native ultrastructure of the red cell cytoskeleton by cryo-electron tomography. Biophys J 101: 2341–2350.
48. DulinskaI, TargoszM, StrojnyW, LekkaM, CzubaP, et al. (2006) Stiffness of normal and pathological erythrocytes studied by means of atomic force microscopy. J Biochem Biophys Methods 66: 1–11.
49. LamWA, RosenbluthMJ, FletcherDA (2008) Increased leukaemia cell stiffness is associated with symptoms of leucostasis in paediatric acute lymphoblastic leukaemia. Br J Haematol 142: 497–501.
50. HuynhJ, NishimuraN, RanaK, PeloquinJM, CalifanoJP, et al. (2011) Age-related intimal stiffening enhances endothelial permeability and leukocyte transmigration. Sci Transl Med 3: 112ra122.
51. GiardiniPA, FletcherDA, TheriotJA (2003) Compression forces generated by actin comet tails on lipid vesicles. Proc Natl Acad Sci U S A 100: 6493–6498.
52. RajabianT, GavicherlaB, HeisigM, Muller-AltrockS, GoebelW, et al. (2009) The bacterial virulence factor InlC perturbs apical cell junctions and promotes cell-to-cell spread of Listeria. Nat Cell Biol 11: 1212–1218.
53. HardhamAR, JonesDA, TakemotoD (2007) Cytoskeleton and cell wall function in penetration resistance. Curr Opin Plant Biol 10: 342–348.
54. Delorme-WalkerV, AbrivardM, LagalV, AndersonK, PerazziA, et al. (2012) Toxofilin upregulates the host cortical actin cytoskeleton dynamics, facilitating Toxoplasma invasion. J Cell Sci 125: 4333–4342.
55. GonzalezV, CombeA, DavidV, MalmquistNA, DelormeV, et al. (2009) Host cell entry by apicomplexa parasites requires actin polymerization in the host cell. Cell Host Microbe 5: 259–272.
56. OnderdonkAB, DelaneyML, DuBoisAM, AllredEN, LevitonA (2008) Detection of bacteria in placental tissues obtained from extremely low gestational age neonates. Am J Obstet Gynecol 198: 110 e111–117.
57. PereiraL, MaidjiE, McDonaghS, GenbacevO, FisherS (2003) Human cytomegalovirus transmission from the uterus to the placenta correlates with the presence of pathogenic bacteria and maternal immunity. J Virol 77: 13301–13314.
58. CardenasI, MorG, AldoP, LangSM, StabachP, et al. (2011) Placental viral infection sensitizes to endotoxin-induced pre-term labor: a double hit hypothesis. Am J Reprod Immunol 65: 110–117.
59. CardenasI, MeansRE, AldoP, KogaK, LangSM, et al. (2010) Viral infection of the placenta leads to fetal inflammation and sensitization to bacterial products predisposing to preterm labor. J Immunol 185: 1248–1257.
60. CrockerIP, TannerOM, MyersJE, BulmerJN, WalravenG, et al. (2004) Syncytiotrophoblast degradation and the pathophysiology of the malaria-infected placenta. Placenta 25: 273–282.
61. HromatkaBS, NgelezaS, AdibiJJ, NilesRK, TshefuAK, et al. (2013) Histopathologies, immunolocalization, and a glycan binding screen provide insights into Plasmodium falciparum interactions with the human placenta. Biol Reprod 88: 154.
62. DuasoJ, RojoG, JanaF, GalantiN, CabreraG, et al. (2011) Trypanosoma cruzi induces apoptosis in ex vivo infected human chorionic villi. Placenta 32: 356–361.
63. BulterysPL, ChaoA, DalaiSC, ZinkMC, DushimimanaA, et al. (2011) Placental malaria and mother-to-child transmission of human immunodeficiency virus-1 in rural Rwanda. Am J Trop Med Hyg 85: 202–206.
64. DupressoirA, LavialleC, HeidmannT (2012) From ancestral infectious retroviruses to bona fide cellular genes: role of the captured syncytins in placentation. Placenta 33: 663–671.
65. StarkRW, DrobekT, HecklWM (2001) Thermomechanical noise of a free v-shaped cantilever for atomic-force microscopy. Ultramicroscopy 86: 207–215.
66. MahaffyRE, ParkS, GerdeE, KasJ, ShihCK (2004) Quantitative analysis of the viscoelastic properties of thin regions of fibroblasts using atomic force microscopy. Biophys J 86: 1777–1793.
67. MandersEM, StapJ, BrakenhoffGJ, van DrielR, AtenJA (1992) Dynamics of three-dimensional replication patterns during the S-phase, analysed by double labelling of DNA and confocal microscopy. J Cell Sci 103 (Pt 3) 857–862.
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Hygiena a epidemiológia Infekčné lekárstvo LaboratóriumČlánok vyšiel v časopise
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