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Effects of Maternal Exposure to Ultrafine Carbon Black on Brain Perivascular Macrophages and Surrounding Astrocytes in Offspring Mice
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![Figure 5 Transmission electron micrographs of perivascular macrophages (PVMs) and astrocytic end-foot. All scale bars represent 2 μm. A–C: Electron micrograph of perivascular regions of the cerebral cortex (grey matter) of (A, B) 6- and (C) 12-week-old mouse in the control group. (A, C) Perivascular macrophages [PVM] were found between endothelial cells and glia limitans with many round lysosomal granules [LG] of moderate intensity and some pale vacuoles. (B, C) The astrocytic end-foot [AE] was attached to a endothelial cells [EC] and a perivascular macrophage. D, E: Electron micrographs of perivascular regions of the cerebral cortex (grey matter) of (D) 6- and (E) 12-week-old UfCB-exposed offspring mouse. (D) Arrow head: Crescent-shaped spaces, an ultrastructural feature of apoptotic bodies [57], of EC were shown. (E) Honeycomb-like structured lysosomal granules (*) were shown in the perivascular macrophages [PVM]. (E) Severe swelling of astrocytic end-feet (**) was found at sites attached to perivascular macrophages with denatured granules.](/paper-figures/f4dae6e07d8749cbaf843fdcddcb7657/effects-of-maternal-exposure-to-ultrafine-carbon-black-on-brain-perivascular-figure-5.jpg)


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“They can serve as an extremely sensitive marker of maternal exposure to low doses of NPs for prediction of their developmental toxicity [170].”
From Particle toxicology and health - where are we? (2019) · cites this paper as [170]
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Mato, M., Ookawara, S., Sakamoto, A., Aikawa, E., Ogawa, T., Mitsuhashi, U., Masuzawa, T., Suzuki, H., Honda, M., Yazaki, Y., et al. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.8.3269 · Cited by 187
Research works printed but not linked: 52
- I Galea, 2005, Mannose receptor expression specifically reveals perivascular macrophages in normal, injured, and diseased mouse brain, Glia, 49, 375, 10.1002/glia.20124 · DOI
- WK Kim, 2006, CD163 identifies perivascular macrophages in normal and viral encephalitic brains and potential precursors to perivascular macrophages in blood, Am J Pathol, 168, 822, 10.2353/ajpath.2006.050215 · DOI · Paper page
- K Williams, 2001, Central nervous system perivascular cells are immunoregulatory cells that connect the CNS with the peripheral immune system, Glia, 36, 156, 10.1002/glia.1105 · DOI · Paper page
- Peters A, Palay SL, Webster HD (1976) The fine structure of thenervous system: the neurons and supporting cells. Philadelphia: WB Saunders.
- MB Graeber, 1992, Ultrastructural location of major histocompatibility complex(MHC) class II positive perivascular cells in histologically normal human brain, J Neuropathol Exp Neurol, 51, 303, 10.1097/00005072-199205000-00009 · DOI
- WJ Streit, 1993, Heterogeneity of microglial and perivascular cell populations: insights gained from the facial nucleus paradigm, Glia, 7, 68, 10.1002/glia.440070112 · DOI
- H Lassmann, 1991, Microglial cells are a component of the perivascular glia limitans, J Neurosci Res, 28, 236, 10.1002/jnr.490280211 · DOI
- H Lassmann, 1993, Bone marrow derived elements and resident microglia in brain inflammation, Glia, 7, 19, 10.1002/glia.440070106 · DOI
- HF Cserr, 1974, Bulk flow of interstitial fluid after intracranial injection of blue dextran 2000, Exp Neurol, 45(1), 50, 10.1016/0014-4886(74)90099-5 · DOI
- RO Weller, 1992, Pathways of fluid drainage from the brain—morphological aspects and immunological significance in rat and man, Brain Pathol, 2(4), 277, 10.1111/j.1750-3639.1992.tb00704.x · DOI
- ET Zhang, 1992, Directional and compartmentalised drainage of interstitial fluid and cerebrospinal fluid from the rat brain, Acta Neuropathol, 83(3), 233, 10.1007/BF00296784 · DOI
- JJ Iliff, 2012, A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid β, Sci Transl Med 15, 4(147), 147
- J Serrats, 2010, Dual roles for perivascular macrophages in immune-to-brain signaling, Neuron, 65, 94, 10.1016/j.neuron.2009.11.032 · DOI · Paper page
- S Kida, 1993, Perivascular cells act as scavengers in the cerebral perivascular spaces and remain distinct from pericytes, microglia and macrophages, Acta Neuropathol (Berl), 85, 646, 10.1007/BF00334675 · DOI · Paper page
- BO Fabriek, 2005, CD163-positive perivascular macrophages in the human CNS express molecules for antigen recognition and presentation, Glia, 51, 297, 10.1002/glia.20208 · DOI
- K Donaldson, 2005, Combustion-derived nanoparticles: a review of their toxicology following inhalation exposure, Part Fibre Toxicol, 21;2, 10, 10.1186/1743-8977-2-10 · DOI
- G Oberdörster, 2005, Nanotoxicology: an emerging discipline evolving from studies of ultrafine particles, Environ Health Perspect, 113(7), 823, 10.1289/ehp.7339 · DOI · Paper page
- A Nel, 2006, Toxic potential of materials at the nanolevel, Science 3, 311(5761), 622, 10.1126/science.1114397 · DOI · Paper page
- S Yamamoto, 2006, Brain cytokine and chemokine mRNA expression in mice induced by intranasal instillation with ultrafine carbon black, Toxicol Lett, 25;163(2), 153
- LK Vesterdal, 2010, Pulmonary exposure to carbon black nanoparticles and vascular effects, Part Fibre Toxicol, 5;7, 33, 10.1186/1743-8977-7-33 · DOI
- K Peters, 2004, Effects of nano-scaled particles on endothelial cell function in vitro: studies on viability, proliferation and inflammation, J Mater Sci Mater Med, 15(4), 321, 10.1023/B:JMSM.0000021095.36878.1b · DOI
- Stone V, Johnston H, Clift MJ (2007) Air pollution, ultrafine and nanoparticle toxicology: cellular and molecular interactions. IEEE Trans Nanobiosci <volume>6</volume>: ; 331–340.
- G Oberdörster, 2002, Extrapulmonary translocation of ultrafine carbon particles following whole-body inhalation exposure of rats, J Toxicol Environ Health A, 65, 1531, 10.1080/00984100290071658 · DOI · Paper page
- WG Kreyling, 2002, Translocation of ultrafine insoluble iridium particles from lung epithelium to extrapulmonary organs is size dependent but very low, J Toxicol Environ Health A, 65, 1513, 10.1080/00984100290071649 · DOI · Paper page
- Takeda K, Suzuki K, Ishihara A, Kubo-Irie M, Fujimoto R, T, et al. (2009) Nanoparticles transferred from pregnant mice to their offspring can damage the genital and cranial nerve systems. Jounal if Health Science 55(1): 95–102 · DOI · Paper page
- M Sugamata, 2006, Maternal Diesel Exhaust Exposure Damages Newborn Murine Brains, Journal of Health Science, 52, 82, 10.1248/jhs.52.82 · DOI
- Jackson P, Vogel U, Wallin H, Hougaard KS (2011) Maternal Exposure to Particulate Air Pollution and Engineered Nanoparticles: Reproductive and Developmental Effects. In: Anca, M M, editor. Air Pollution - New Developments. Rijeka University Campus Step Ri. pp. 59–84. · DOI
- AT Saber, 2011, Inflammatory and genotoxic effects of nanoparticles designed for inclusion in paints and lacquers, Nanotoxicology, 6(5), 453
- NR Jacobsen, 2007, Increased mutant frequency by carbon black, but not quartz, in the lacZ and cII transgenes of muta mouse lung epithelial cells, Environ Mol Mutagen, 48(6), 451, 10.1002/em.20300 · DOI
- NR Jacobsen, 2011, Mutation spectrum in FE1-MUTA(TM) Mouse lung epithelial cells exposed to nanoparticulate carbon black, Environ Mol Mutagen, 52(4), 331, 10.1002/em.20629 · DOI
- Wilson JG (1972) Environmental effects on development-teratology. In: N F Affli, edtor. Pathophysiology of gestation, <volume>vol. II. </volume> New York: Academic. pp. 270–320.
- A1 Pietroiusti, 2011, Low doses of pristine and oxidized single-wall carbon nanotubes affect mammalian embryonic development, ACS Nano, 28;5(6), 4624, 10.1021/nn200372g · DOI
- M Umezawa, 2011, Maternal exposure to carbon black nanoparticle increases collagen type VIII expression in the kidney of offspring, J Toxicol Sci, 36(4), 461, 10.2131/jts.36.461 · DOI
- C Kilkenny, 2010, Animal research: reporting in vivo experiments: the ARRIVE guidelines, Br J Pharmacol, 160, 1577, 10.1111/j.1476-5381.2010.00872.x · DOI · Paper page
- M Mato, 1979, A simple method for observation of capillary nets in rat brain cortex, Experientia, 15;35(4), 501, 10.1007/BF01922731 · DOI
- GJ Guillemin, 2004, Microglia, macrophages, perivascular macrophages, and pericytes: a review of function and identification, J Leukoc Biol, 75(3), 388, 10.1189/jlb.0303114 · DOI
- M Cavaglia, 2001, Regional variation in brain capillary density and vascular response to ischemia, Brain Res, 10;910(1–2), 81, 10.1016/S0006-8993(01)02637-3 · DOI
- M Mato, 2002, Inclusions in novel perivascular macrophages (Mato's fluorescent granular perithelial cells) and neurons in the cerebral cortex of Hex A- and Hex B-deficient mice, Acta Neuropathol, 103, 119, 10.1007/s004010100441 · DOI
- T Nakazawa, 2006, Acceleration of Age-related Changes in the Granules of Perivascular Macrophages from the Brain of Senescence Accelerated Mice (SAM), J Tokyo Wom Med Univ, 76, 82
- T Mato, 2009, Beneficial Effects of Cocoa in Perivascular Mato Cells of Cerebral Arterioles in SHR-SP (Izm) Rats, J Clin Biochem Nutr, 44, 142, 10.3164/jcbn.08-209 · DOI
- MV Sofroniew, 2010, Astrocytes: biology and pathology, Acta Neuropathol, 119, 7, 10.1007/s00401-009-0619-8 · DOI · Paper page
- AV Molofsky, 2012, Astrocytes and disease: a neurodevelopmental perspective, Genes Dev, 26, 891, 10.1101/gad.188326.112 · DOI · Paper page
- I Klatzo, 1976, Presidental address. Neuropathological aspects of brain edema, J Neuropathol Exp Neurol 1967, 26, 1, 10.1097/00005072-196701000-00001 · DOI
- HH Tsai, 2012, Regional astrocyte allocation regulates CNS synaptogenesis and repair, Science, 337(6092), 358, 10.1126/science.1222381 · DOI
- K BéruBé, 2007, Combustion-derived nanoparticles: mechanisms of pulmonary toxicity, Clin Exp Pharmacol Physiol, 34(10), 1044, 10.1111/j.1440-1681.2007.04733.x · DOI
- T Stoeger, 2009, Deducing in vivo toxicity of combustion-derived nanoparticles from a cell-free oxidative potency assay and metabolic activation of organic compounds, Environ Health Perspect, 117(1), 54, 10.1289/ehp.11370 · DOI
- P Wick, 2010, Barrier capacity of human placenta for nanosized materials, Environ Health Perspect, 118(3), 432, 10.1289/ehp.0901200 · DOI · Paper page
- Hougaard KS, Fadeel B, Gulumian M, Kagan VE, Savolainen KM (2011) Developmental toxicity of engineered nanoparticles. In: Ramesh CG, editor. Reproductive and Developmental Toxicology. Academic Press, San Diego. pp. 269–290. · DOI
- P Jackson, 2012, Pulmonary exposure to carbon black by inhalation or instillation in pregnant mice: effects on liver DNA strand breaks in dams and offspring, Nanotoxicology, 6(5), 486, 10.3109/17435390.2011.587902 · DOI
- Kannan S, Misra DP, Dvonch JT, Krishnakumar A (2007) Exposures to airborne particulate matter and adverse perinatal outcomes: a biologically plausible mechanistic framework for exploring potential. Cien. Saude Colet. 12, 1591–1602. · DOI
- Yokota S, Hori H, Umezawa M, Kubota N, Niki R, et al. (2013) Gene expression changes in the olfactory bulb of mice induced by exposure to diesel exhaust are dependent on animal rearing environment. PLoS One 5; 8 (8) · DOI
- T Ihara, 1998, The process of ultrastructural changes from nuclei to apoptotic body, Virchows Arch, 433(5), 443, 10.1007/s004280050272 · DOI
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Particle toxicology and health - where are we?
Riediker, M., Zink, D., Kreyling, W., Oberdörster, G., Elder, A., Graham, U., Lynch, I., Duschl, A., Ichihara, G., Ichihara, S., et al. (2019) · Particle and Fibre Toxicology · doi:10.1186/s12989-019-0302-8 · Cited by 237
Self-citationMorris-Schaffer, K., Merrill, A., Jew, K., Wong, C., Conrad, K., Harvey, K., Marvin, E., Sobolewski, M., Oberdörster, G., Elder, A., et al. (2019) · Particle and Fibre Toxicology · doi:10.1186/s12989-019-0293-5 · Cited by 44
Metadata
- Authors
- Onoda, A., Umezawa, M., Takeda, K., Ihara, T., & Sugamata, M.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2014-04-10
- Volume
- 9
- Issue
- 4
- Pages
- e94336
- ISSN
- 1932-6203
- PMC
- PMC3983141
- Cited by
- 56
- References
- 1
- Language
- en
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