References
-
Akdis, M., Aab, A., Altunbulakli, C., Azkur, K., Costa, R. A., Crameri, R., Duan, S., Eiwegger, T., Eljaszewicz, A., Ferstl, R., Frei, R., Garbani, M., Globinska, A., Hess, L., Huitema, C., Kubo, T., Komlosi, Z., Konieczna, P., Kovacs, N., Kucuksezer, U. C., Meyer, N., Morita, H., Olzhausen, J., O'Mahony, L., Pezer, M., Prati, M., Rebane, A., Rhyner, C., Rinaldi, A., Sokolowska, M., Stanic, B., Sugita, K., Treis, A., van de Veen, W., Wanke, K., Wawrzyniak, M., Wawrzyniak, P., Wirz, O. F., Zakzuk, J. S. & Akdis, C. A. 2016. Interleukins (from IL-1 to IL-38), interferons, transforming growth factor
${\beta}$ , and TNF-${\alpha}$ : receptors, functions, and roles in diseases. J. Allergy Clin. Immunol. 138:984-1010. https://doi.org/10.1016/j.jaci.2016.06.033 - Barker, J. N. W. N., Griffiths, C. E. M., Nickoloff, B. J., Mitra, R. S., Dixit, V. M. & Nickoloff, B. J. 1991. Keratinocytes as initiators of inflammation. Lancet 337:211-214. https://doi.org/10.1016/0140-6736(91)92168-2
-
Bekki, K., Ito, T., Yoshida, Y., He, C., Arashidani, K., He, M., Sun, G., Zeng, Y., Sone, H., Kunugita, N. & Ichinose, T. 2016.
$PM_{2.5}$ collected in China causes inflammatory and oxidative stress responses in macrophages through the multiple pathways. Environ. Toxicol. Pharmacol. 45:362-369. https://doi.org/10.1016/j.etap.2016.06.022 - Choi, J. C., Lee, M., Chun, Y., Kim, J. & Oh, S. 2001. Chemical composition and source signature of spring aerosol in Seoul, Korea. J. Geophys. Res. Atmos. 106:18067-18074. https://doi.org/10.1029/2001JD900090
- Doelman, C. J. A., Leurs, R., Oosterom, W. C. & Bast, A. 1990. Mineral dust exposure and free radical-mediated lung damage. Exp. Lung Res. 16:41-55. https://doi.org/10.3109/01902149009064698
- Dooms-Goossens, A. E., Debusschere, K. M., Gevers, D. M., Dupre, K. M., Degreef, H. J., Loncke, J. P. & Snauwaert, J. E. 1986. Contact dermatitis caused by airborne agents. J. Am. Acad. Dermatol. 15:1-10. https://doi.org/10.1016/S0190-9622(86)70135-7
- Eom, S.-H., Moon, S.-Y., Lee, D.-S., Kim, H.-J., Park, K., Lee, E.-W., Kim, T. H., Chung, Y.-H., Lee, M.-S. & Kim, Y.-M. 2015. In vitro antiviral activity of dieckol and phlorofucofuroeckol-A isolated from edible brown alga Eisenia bicyclis against murine norovirus. Algae 30:241-246. https://doi.org/10.4490/algae.2015.30.3.241
- Fernando, I. P. S., Kim, M., Son, K. -T., Jeong, Y. & Jeon, Y. -J. 2016a. Antioxidant activity of marine algal polyphenolic compounds: a mechanistic approach. J. Med. Food 19:615-628. https://doi.org/10.1089/jmf.2016.3706
- Fernando, I. P. S., Nah, J. W. & Jeon, Y. J. 2016b. Potential antiinflammatory natural products from marine algae. Environ. Toxicol. Pharmacol. 48:22-30. https://doi.org/10.1016/j.etap.2016.09.023
- Fernando, I. P. S., Sanjeewa, K. K. A., Samarakoon, K. W., Lee, W. W., Kim, H. -S., Kang, N., Ranasinghe, P., Lee, H. -S. & Jeon, Y. -J. 2017a. A fucoidan fraction purified from Chnoospora minima: a potential inhibitor of LPS-in-duced inflammatory responses. Int. J. Biol. Macromol. 104:1185-1193. https://doi.org/10.1016/j.ijbiomac.2017.07.031
- Fernando, I. P. S., Sanjeewa, K. K. A., Samarakoon, K. W., Lee, W. W., Kim, H. -S., Kim, E. -A., Gunasekara, U. K. D. S. S., Abeytunga, D. T. U., Nanayakkara, C., de Silva, E. D., Lee, H. -S. & Jeon, Y. -J. 2017b. FTIR characterization and antioxidant activity of water soluble crude polysaccharides of Sri Lankan marine algae. Algae 32:75-86. https://doi.org/10.4490/algae.2017.32.12.1
- Fujiwara, N. & Kobayashi, K. 2005. Macrophages in Inflammation. Curr. Drug Targets Inflamm. Allergy 4:281-286. https://doi.org/10.2174/1568010054022024
- Han, S. -C., Kang, N. -J., Kang, G. -J., Koh, Y. -S., Hyun, J. -W., Lee, N. -H., Kang, H. -K. & Yoo, E. -S. 2014. 71: Anti-inflammatory effect of diphlorethohydroxycarmalol (DPHC) isolated from lshige okamuarae in vitro and in vivo. Cytokine 70:44-45.
-
Heo, S. -J., Hwang, J. -Y., Choi, J. -I., Han, J. -S., Kim, H. -J. & Jeon, Y. -J. 2009. Diphlorethohydroxycarmalol isolated from Ishige okamurae, a brown algae, a potent
${\alpha}$ -glucosidase and${\alpha}$ -amylase inhibitor, alleviates postprandial hyperglycemia in diabetic mice. Eur. J. Pharmacol. 615:252-256. https://doi.org/10.1016/j.ejphar.2009.05.017 - Heo, S. -J., Kim, J. -P., Jung, W. -K., Lee, N. -H., Kang, H. -S., Jun, E. -M., Park, S. -H., Kang, S. -M., Lee, Y. -J., Park, P. -J. & Jeon, Y. -J. 2008. Identification of chemical structure and free radical scavenging activity of diphlorethohydroxycarmalol isolated from a brown alga, Ishige okamurae. J. Microbiol. Biotechnol. 18:676-681.
- Heo, S. -J., Ko, S. -C., Kang, S. -M., Cha, S. -H., Lee, S. -H., Kang, D. -H., Jung, W. -K., Affan, A., Oh, C. & Jeon, Y. -J. 2010. Inhibitory effect of diphlorethohydroxycarmalol on melanogenesis and its protective effect against UV-B radiation-induced cell damage. Food Chem. Toxicol. 48:1355-1361. https://doi.org/10.1016/j.fct.2010.03.001
- Jalava, P. I., Salonen, R. O., Pennanen, A. S., Sillanpaa, M., Halinen, A. I., Happo, M. S., Hillamo, R., Brunekreef, B., Katsouyanni, K., Sunyer, J. & Hirvonen, M. -R. 2007. Heterogeneities in inflammatory and cytotoxic responses of RAW 264.7 macrophage cell line to urban air coarse, fine, and ultrafine particles from six European sampling campaigns. Inhal. Toxicol. 19:213-225.
- Kandaswami, C., Morin, G. & Sirois, P. 1988. Lipid peroxidation in rat alveolar macrophages exposed to chrysotile fibres. Toxicol. In Vitro 2:117-120. https://doi.org/10.1016/0887-2333(88)90021-5
-
Kim, B. -G., Han, J. -S. & Park, S. -U. 2001. Transport of
$SO_2$ and aerosol over the Yellow sea. Atmos. Environ. 35:727-737. https://doi.org/10.1016/S1352-2310(00)00344-7 - Kim, H. -H., Kim, H. -S., Ko, J. -Y., Kim, C. -Y., Lee, J. -H. & Jeon, Y. -J. 2016. A single-step isolation of useful antioxidant compounds from Ishige okamurae by using centrifugal partition chromatography. Fish. Aquat. Sci. 19:22. https://doi.org/10.1186/s41240-016-0023-y
- Kim, S. -Y., Kim, E. -A., Kang, M. -C., Lee, J. -H., Yang, H. -W., Lee, J. -S., Lim, T. I. & Jeon, Y. -J. 2014. Polyphenol-rich fraction from Ecklonia cava (a brown alga) processing by-product reduces LPS-induced inflammation in vitro and in vivo in a zebrafish model. Algae 29:165-174. https://doi.org/10.4490/algae.2014.29.2.165
- Lee, J. -H., Ko, J. -Y., Oh, J. -Y., Kim, E. -A., Kim, C. -Y. & Jeon, Y. -J. 2015a. Evaluation of phlorofucofuroeckol-A isolated from Ecklonia cava (Phaeophyta) on anti-lipid peroxidation in vitro and in vivo. Algae 30:313-323. https://doi.org/10.4490/algae.2015.30.4.313
- Lee, S. -H., Kang, S. -M., Sok, C. H., Hong, J. T., Oh, J. -Y. & Jeon, Y. -J. 2015b. Cellular activities and docking studies of eckol isolated from Ecklonia cava (Laminariales, Phaeophyceae) as potential tyrosinase inhibitor. Algae 30:163-170.
- Lee, Y. G., Ho, C. -H., Kim, J. -H. & Kim, J. 2015c. Quiescence of Asian dust events in South Korea and Japan during 2012 spring: dust outbreaks and transports. Atmos. Environ. 114:92-101. https://doi.org/10.1016/j.atmosenv.2015.05.035
-
Li, Q. & Verma, I. M. 2002. NF-
${\kappa}B$ regulation in the immune system. Nat. Rev. Immunol. 2:725-734. https://doi.org/10.1038/nri910 -
Monn, C. & Becker, S. 1999. Cytotoxicity and induction of proinflammatory cytokines from human monocytes exposed to fine (
$PM_{2.5}$ ) and coarse particles ($PM_{10}$ -2.5) in outdoor and indoor air. Toxicol. Appl. Pharmacol. 155:245-252. https://doi.org/10.1006/taap.1998.8591 - Moreira dos Santos, C. Y., de Almeida Azevedo, D. & de Aquino Neto, F. R. 2004. Atmospheric distribution of organic compounds from urban areas near a coal-fired power station. Atmos. Environ. 38:1247-1257. https://doi.org/10.1016/j.atmosenv.2003.11.026
- Nel, A. E., Diaz-Sanchez, D., Ng, D., Hiura, T. & Saxon, A. 1998. Enhancement of allergic inflammation by the interaction between diesel exhaust particles and the immune system. J. Allergy Clin. Immunol. 102:539-554. https://doi.org/10.1016/S0091-6749(98)70269-6
- Oh, J. -Y., Fernando, I. P. S. & Jeon, Y. -J. 2016. Potential applications of radioprotective phytochemicals from marine algae. Algae 31:403-414. https://doi.org/10.4490/algae.2016.31.12.1
-
Pozzi, R., De Berardis, B., Paoletti, L. & Guastadisegni, C. 2003. Inflammatory mediators induced by coarse (
$PM_{2.5}$ -10) and fine ($PM_{2.5}$ ) urban air particles in RAW 264.7 cells. Toxicology 183:243-254. https://doi.org/10.1016/S0300-483X(02)00545-0 - Sanjeewa, K. K. A., Fernando, I. P. S., Kim, E. -A., Ahn, G., Jee, Y. & Jeon, Y. -J. 2016a. Anti-inflammatory activity of a sulfated polysaccharide isolated from an enzymatic digest of brown seaweed Sargassum horneri in RAW 264.7 cells. Nutr. Res. Pract. 11:3-10.
- Sanjeewa, K. K. A., Fernando, I. P. S., Samarakoon, K. W., Lakmal, H. H. C., Kim, E.-A., Kwon, O.-N., Dilshara, M. G., Lee, J.-B. & Jeon, Y.-J. 2016b. Anti-inflammatory and anti-cancer activities of sterol rich fraction of cultured marine microalga Nannochloropsis oculata. Algae 31:277-287. https://doi.org/10.4490/algae.2016.31.6.29
- Schuetz, L. 1989. Atmospheric mineral dust: properties and source markers. In Leinen, M. & Sarnthein, M. (Eds.) Paleoclimatology and Paleometeorology: Modern and Past Patterns of Global Atmospheric Transport. Springer Netherlands, Dordrecht, pp. 359-383.
- Schwartz, J., Dockery, D. W. & Neas, L. M. 1996. Is daily mortality associated specifically with fine particles? J. Air Waste Manag. Assoc. 46:927-939. https://doi.org/10.1080/10473289.1996.10467528
- Vallyathan, V., Shi, X., Dalal, N. S., Irr, W. & Castranova, V. 1988. Generation of free radicals from freshly fractured silica dust: potential role in acute silica-induced lung injury. Am. Rev. Respir. Dis. 138:1213-1219. https://doi.org/10.1164/ajrccm/138.5.1213
-
Wijesinghe, W. A. J. P., Kang, M. -C., Lee, W. -W., Lee, H. -S., Kamada, T., Vairappan, C. S. & Jeon, Y. -J. 2014. 5
${\beta}$ -Hydroxypalisadin B isolated from red alga Laurencia snackeyi attenuates inflammatory response in lipopolysaccharide-stimulated RAW 264.7 macrophages. Algae 29:333-341. https://doi.org/10.4490/algae.2014.29.4.333 - Williams, I. R. & Kupper, T. S. 1996. Immunity at the surface: homeostatic mechanisms of the skin immune system. Life Sci. 58:1485-1507. https://doi.org/10.1016/0024-3205(96)00042-2
- Zbytek, B., Mysliwski, A., Slominski, A., Wortsman, J., Wei, E. T. & Mysliwska, J. 2002. Corticotropin-releasing hormone affects cytokine production in human HaCaT keratinocytes. Life Sci. 70:1013-1021. https://doi.org/10.1016/S0024-3205(01)01476-X
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