R. D. Brook, S. Rajagopalan, C. A. Pope, J. R. Brook, A. Bhatnagar et al., Particulate matter air pollution and cardiovascular disease: An update to the scientific statement from the American Heart Association, Circulation, vol.121, pp.2331-2378, 2010.

R. D. Brook and S. Rajagopalan, Chronic air pollution exposure and endothelial dysfunction: What you can't see-can harm you, J. Am. Coll. Cardiol, vol.60, pp.2167-2169, 2012.

D. P. Ramji and T. S. Davies, Cytokines in atherosclerosis: Key players in all stages of disease and promising therapeutic targets, Cytokine Growth. Factor Rev, vol.26, pp.673-685, 2015.

A. O. Lawal, L. M. Davids, and J. L. Marnewick, Diesel exhaust particles and endothelial cells dysfunction: An update, Toxicol. In Vitro, vol.32, pp.92-104, 2016.
DOI : 10.1016/j.tiv.2015.12.015

B. Urch, J. R. Brook, D. Wasserstein, R. D. Brook, S. Rajagopalan et al., Relative contributions of PM2.5 chemical constituents to acute arterial vasoconstriction in humans, Inhal. Toxicol, vol.16, pp.345-352, 2004.

P. Moller, D. V. Christophersen, N. R. Jacobsen, A. Skovmand, A. C. Gouveia et al., Atherosclerosis and vasomotor dysfunction in arteries of animals after exposure to combustion-derived particulate matter or nanomaterials, Crit. Rev. Toxicol, vol.46, pp.437-476, 2016.

H. Tornqvist, N. L. Mills, M. Gonzalez, M. R. Miller, S. D. Robinson et al., Persistent endothelial dysfunction in humans after diesel exhaust inhalation, Am. J. Respir. Crit. Care Med, vol.176, pp.395-400, 2007.

S. Kawasaki, H. Takizawa, K. Takami, M. Desaki, H. Okazaki et al., Benzene-extracted components are important for the major activity of diesel exhaust particles: Effect on interleukin-8 gene expression in human bronchial epithelial cells, Am. J. Respir. Cell Mol. Biol, vol.24, pp.419-426, 2001.

V. Bonvallot, A. Baeza-squiban, A. Baulig, S. Brulant, S. Boland et al., Organic compounds from diesel exhaust particles elicit a proinflammatory response in human airway epithelial cells and induce cytochrome p450 1A1 expression, Am. J. Respir. Cell Mol. Biol, vol.25, pp.515-521, 2001.

A. I. Totlandsdal, J. I. Herseth, A. K. Bolling, A. Kubatova, A. Braun et al., Differential effects of the particle core and organic extract of diesel exhaust particles, Toxicol. Lett, vol.208, pp.262-268, 2012.

A. J. Keebaugh, C. Sioutas, P. Pakbin, J. J. Schauer, L. B. Mendez et al., Is atherosclerotic disease associated with organic components of ambient fine particles?, Sci. Total Environ, vol.533, pp.69-75, 2015.

O. Alshaarawy, H. A. Elbaz, and M. E. Andrew, The association of urinary polycyclic aromatic hydrocarbon biomarkers and cardiovascular disease in the US population, Environ. Int, pp.174-178, 2016.

L. Trasande, E. M. Urbina, M. Khoder, M. Alghamdi, I. Shabaj et al., Polycyclic aromatic hydrocarbons, brachial artery distensibility and blood pressure among children residing near an oil refinery, Environ. Res, vol.136, pp.133-140, 2015.
DOI : 10.1016/j.envres.2014.08.038

URL : http://europepmc.org/articles/pmc5274701?pdf=render

C. E. Bostrom, P. Gerde, A. Hanberg, B. Jernstrom, C. Johansson et al., Cancer risk assessment, indicators, and guidelines for polycyclic aromatic hydrocarbons in the ambient air, Environ. Health Perspect, vol.110, pp.451-488, 2002.

K. Yang, X. Jiang, S. Cheng, C. Chen, X. Cao et al., Effects of coke oven emissions and benzo[a]pyrene on blood pressure and electrocardiogram in coke oven workers, J. Occup. Health, vol.59, pp.1-7, 2017.

A. Penn, G. Murphy, S. Barker, W. Henk, and L. Penn, Combustion-derived ultrafine particles transport organic toxicants to target respiratory cells, Environ. Health Perspect, vol.113, pp.956-963, 2005.
DOI : 10.1289/ehp.7661

URL : http://europepmc.org/articles/pmc1280333?pdf=render

P. Gerde, B. A. Muggenburg, M. Lundborg, and A. R. Dahl, The rapid alveolar absorption of diesel soot-adsorbed benzo[a]pyrene: Bioavailability, metabolism and dosimetry of an inhaled particle-borne carcinogen, Carcinogenesis, vol.22, pp.741-749, 2001.

B. C. Brinchmann, T. Skuland, M. H. Rambøl, K. Szoke, J. E. Brinchmann et al., Lipophilic components of diesel exhaust particles induce pro-inflammatory responses in human endothelial cells through AhR dependent pathway(s), Part. Fibre Toxicol, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01863051

C. Esser and A. Rannug, The aryl hydrocarbon receptor in barrier organ physiology, immunology, and toxicology, Pharmacol. Rev, vol.67, pp.259-279, 2015.

L. P. Nguyen and C. A. Bradfield, The search for endogenous activators of the aryl hydrocarbon receptor, Chem. Res. Toxicol, vol.21, pp.102-116, 2008.

J. Savouret, A. Berdeaux, and R. E. Casper, The aryl hydrocarbon receptor and its xenobiotic ligands-triggers CVD, Nutr. Metab. Cardiovasc. Dis, vol.13, pp.104-113, 2003.

P. G. Kopf, J. K. Huwe, and M. K. Walker, Hypertension, cardiac hypertrophy, and impaired vascular relaxation induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin are associated with increased superoxide, Cardiovasc. Toxicol, vol.8, pp.181-193, 2008.
DOI : 10.1007/s12012-008-9027-x

URL : http://europepmc.org/articles/pmc2648846?pdf=render

M. S. Denison, A. A. Soshilov, G. He, D. E. Degroot, and B. Zhao, Exactly the same but different: Promiscuity and diversity in the molecular mechanisms of action of the aryl hydrocarbon (dioxin) receptor, Toxicol. Sci, vol.124, pp.1-22, 2011.

E. Guyot, A. Chevallier, R. Barouki, and X. Coumoul, The AhR twist: Ligand-dependent AhR signaling and pharmaco-toxicological implications, Drug. Discov. Today, vol.18, pp.479-486, 2013.

Y. Tian, A. B. Rabson, and M. A. Gallo, Ah receptor and NF-kappaB interactions: Mechanisms and physiological implications, Chem. Biol. Interact, vol.141, pp.97-115, 2002.
DOI : 10.1016/s0009-2797(02)00068-6

F. Matsumura, The significance of the nongenomic pathway in mediating inflammatory signaling of the dioxin-activated Ah receptor to cause toxic effects, Biochem. Pharmacol, vol.77, pp.608-626, 2009.

C. Tomkiewicz, L. Herry, L. C. Bui, C. Metayer, M. Bourdeloux et al., The aryl hydrocarbon receptor regulates focal adhesion sites through a non-genomic FAK/Src pathway, Oncogene, vol.32, pp.1811-1820, 2013.

S. L. Sandow, S. Senadheera, T. H. Grayson, D. G. Welsh, and T. V. Murphy, Calcium and endothelium-mediated vasodilator signaling, Adv. Exp. Med. Biol, vol.740, pp.811-831, 2012.
DOI : 10.1007/978-94-007-2888-2_36

P. Moller, L. Mikkelsen, L. K. Vesterdal, J. K. Folkmann, L. Forchhammer et al., Hazard identification of particulate matter on vasomotor dysfunction and progression of atherosclerosis, Crit. Rev. Toxicol, vol.41, pp.339-368, 2011.

S. L. Sandow, R. E. Haddock, C. E. Hill, P. S. Chadha, P. M. Kerr et al., What's where and why at a vascular myoendothelial microdomain signalling complex, Clin. Exp. Pharmacol. Physiol, vol.36, pp.67-76, 2009.

D. E. Clapham, Calcium signaling, Cell, vol.131, pp.1047-1058, 2007.

X. Yao and C. J. Garland, Recent developments in vascular endothelial cell transient receptor potential channels, Circ. Res, vol.97, pp.853-863, 2005.

Z. Majkova, M. Toborek, and B. Hennig, The role of caveolae in endothelial cell dysfunction with a focus on nutrition and environmental toxicants, J. Cell Mol. Med, vol.14, pp.2359-2370, 2010.

S. Chakraborty and G. Hasan, IP3R, store-operated Ca 2+ entry and neuronal Ca2+ homoeostasis in Drosophila, Biochem. Soc. Trans. 2012, vol.40, pp.279-281

Y. Liao, C. Erxleben, J. Abramowitz, V. Flockerzi, M. X. Zhu et al., Functional interactions among Orai1, TRPCs, and STIM1 suggest a STIM-regulated heteromeric Orai/TRPC model for SOCE/Icrac channels, Proc. Natl. Acad. Sci, vol.105, pp.2895-2900, 2008.
DOI : 10.1073/pnas.0712288105

URL : https://www.pnas.org/content/pnas/105/8/2895.full.pdf

I. S. Ambudkar, L. B. Souza, H. L. Ong, . Trpc1, . Orai1 et al., Friends in tight spaces. Cell Calcium, vol.63, pp.33-39, 2017.

J. W. Putney and T. Tomita, Phospholipase C signaling and calcium influx, Adv. Biol. Regul, vol.52, pp.152-164, 2012.
DOI : 10.1016/j.advenzreg.2011.09.005

URL : http://europepmc.org/articles/pmc3560308?pdf=render

M. W. Fariss, M. I. Gilmour, C. A. Reilly, W. Liedtke, and A. J. Ghio, Emerging mechanistic targets in lung injury induced by combustion-generated particles, Toxicol. Sci, vol.132, pp.253-267, 2013.
DOI : 10.1093/toxsci/kft001

URL : https://academic.oup.com/toxsci/article-pdf/132/2/253/10935616/kft001.pdf

J. Li, P. Kanju, M. Patterson, W. L. Chew, S. H. Cho et al., TRPV4-mediated calcium influx into human bronchial epithelia upon exposure to diesel exhaust particles, Environ. Health Perspect, vol.119, pp.784-793, 2011.
DOI : 10.1289/ehp.1002807

URL : http://europepmc.org/articles/pmc3114812?pdf=render

K. Smedlund, M. Bah, and G. Vazquez, On the role of endothelial TRPC3 channels in endothelial dysfunction and cardiovascular disease, Cardiovasc. Hematol. Agents Med. Chem, vol.10, pp.265-274, 2012.

S. Earley and J. E. Brayden, Transient receptor potential channels in the vasculature, Physiol. Rev, vol.95, pp.645-690, 2015.

M. N. Sullivan and S. Earley, TRP channel Ca 2+ sparklets: Fundamental signals underlying endothelium-dependent hyperpolarization, Am. J. Physiol. Cell Physiol, vol.305, pp.999-1008, 2013.
DOI : 10.1152/ajpcell.00273.2013

URL : http://europepmc.org/articles/pmc3840200

S. Earley, TRPA1 channels in the vasculature, Br. J. Pharmacol, vol.167, pp.13-22, 2012.
DOI : 10.1111/j.1476-5381.2012.02018.x

URL : https://bpspubs.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1476-5381.2012.02018.x

S. Barath, N. L. Mills, M. Lundback, H. Tornqvist, A. J. Lucking et al., Impaired vascular function after exposure to diesel exhaust generated at urban transient running conditions, Part. Fibre Toxicol, 2010.
DOI : 10.1186/1743-8977-7-19

URL : https://particleandfibretoxicology.biomedcentral.com/track/pdf/10.1186/1743-8977-7-19

A. Mayati, E. Le-ferrec, D. Lagadic-gossmann, and O. Fardel, Aryl hydrocarbon receptor-independent up-regulation of intracellular calcium concentration by environmental polycyclic aromatic hydrocarbons in human endothelial HMEC-1 cells, Environ. Toxicol, vol.27, pp.556-562, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00680889

A. Mayati, E. Le-ferrec, J. A. Holme, O. Fardel, D. Lagadic-gossmann et al., Calcium signaling and beta2-adrenergic receptors regulate 1-nitropyrene induced CXCL8 responses in BEAS-2B cells, Toxicol. Vitro, vol.28, pp.1153-1157, 2014.
DOI : 10.1016/j.tiv.2014.05.012

URL : https://hal-univ-rennes1.archives-ouvertes.fr/hal-01058607/file/Calcium_Signaling_and_I_2-Adrenergic_Receptors-final.pdf

C. E. Deering-rice, E. G. Romero, D. Shapiro, R. W. Hughen, A. R. Light et al., Electrophilic components of diesel exhaust particles (DEP) activate transient receptor potential ankyrin-1 (TRPA1): a probable mechanism of acute pulmonary toxicity for DEP, Chem. Res. Toxicol, vol.24, pp.950-959, 2011.

S. Z. Xu, F. Zeng, G. Boulay, C. Grimm, C. Harteneck et al., Block of TRPC5 channels by 2-aminoethoxydiphenyl borate: A differential, extracellular and voltage-dependent effect, Br. J. Pharmacol, vol.145, pp.405-414, 2005.

H. Z. Hu, Q. Gu, C. Wang, C. K. Colton, J. Tang et al., 2-aminoethoxydiphenyl borate is a common activator of TRPV1, TRPV2, and TRPV3, J. Biol. Chem, vol.279, pp.35741-35748, 2004.

B. Pani and B. B. Singh, Lipid rafts/caveolae as microdomains of calcium signaling, Cell Calcium, vol.45, pp.625-633, 2009.

P. Wiggins and R. Phillips, Membrane-protein interactions in mechanosensitive channels, Biophys. J, vol.88, pp.880-902, 2005.

R. A. Cooper, Influence of increased membrane cholesterol on membrane fluidity and cell function in human red blood cells, J. Supramol. Struct, vol.8, pp.413-430, 1978.

A. O. Lawal, M. Zhang, M. Dittmar, A. Lulla, and J. A. Araujo, Heme oxygenase-1 protects endothelial cells from the toxicity of air pollutant chemicals, Toxicol. Appl. Pharmacol, vol.284, pp.281-291, 2015.

K. W. Gong, W. Zhao, N. Li, B. Barajas, M. Kleinman et al., Air-pollutant chemicals and oxidized lipids exhibit genome-wide synergistic effects on endothelial cells, Genome Biol, vol.8, 2007.
DOI : 10.1186/gb-2007-8-7-r149

URL : https://genomebiology.biomedcentral.com/track/pdf/10.1186/gb-2007-8-7-r149

D. M. Demarini, L. R. Brooks, S. H. Warren, T. Kobayashi, M. I. Gilmour et al., Bioassay-directed fractionation and salmonella mutagenicity of automobile and forklift diesel exhaust particles, Environ. Health Perspect, vol.112, pp.814-819, 2004.

M. S. Kim, W. Zeng, J. P. Yuan, D. M. Shin, P. F. Worley et al., Native Store-operated Ca 2+ Influx Requires the Channel Function of Orai1 and TRPC1, J. Biol. Chem, vol.284, pp.9733-9741, 2009.

G. U. Ahmmed, D. Mehta, S. Vogel, M. Holinstat, B. C. Paria et al., Protein kinase Calpha phosphorylates the TRPC1 channel and regulates store-operated Ca 2+ entry in endothelial cells, J. Biol. Chem, vol.279, pp.20941-20949, 2004.

T. C. Ho, N. A. Horn, T. Huynh, L. Kelava, and J. B. Lansman, Evidence TRPV4 contributes to mechanosensitive ion channels in mouse skeletal muscle fibers, Channels, vol.6, pp.246-254, 2012.

A. Singh, M. E. Hildebrand, E. Garcia, and T. P. Snutch, The transient receptor potential channel antagonist SKF96365 is a potent blocker of low-voltage-activated T-type calcium channels, Br. J. Pharmacol, vol.160, pp.1464-1475, 2010.

V. Hartmannsgruber, W. T. Heyken, M. Kacik, A. Kaistha, I. Grgic et al., Arterial response to shear stress critically depends on endothelial TRPV4 expression, PLoS ONE, vol.2, 2007.
DOI : 10.1371/journal.pone.0000827

URL : https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0000827&type=printable

Y. Liao, N. W. Plummer, M. D. George, J. Abramowitz, M. X. Zhu et al., A role for Orai in TRPC-mediated Ca 2+ entry suggests that a TRPC:Orai complex may mediate store and receptor operated Ca 2+ entry, Proc. Natl. Acad. Sci, vol.106, pp.3202-3206, 2009.

J. L. Marlowe and A. Puga, Aryl hydrocarbon receptor, cell cycle regulation, toxicity, and tumorigenesis, J. Cell. Biochem, vol.96, pp.1174-1184, 2005.
DOI : 10.1002/jcb.20656

URL : https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcb.20656

B. Dong and F. Matsumura, Roles of cytosolic phospholipase A2 and Src kinase in the early action of 2,3,7,8-tetrachlorodibenzo-p-dioxin through a nongenomic pathway in MCF10A cells, Mol. Pharmacol, vol.74, pp.255-263, 2008.

A. Puga, A. Hoffer, S. Zhou, J. M. Bohm, G. D. Leikauf et al., Sustained Increase in Intracellular Free Calcium and Activation of Cyclooxygenase-2 Expression in Mouse Hepatoma Cells Treated with Dioxin, Biochem. Pharmacol, vol.54, pp.1287-1296, 1997.

J. Rey-barroso, The Dioxin receptor modulates Caveolin-1 mobilization during directional migration: Role of cholesterol, Cell Commun. Signal, vol.12, 2014.

Y. Iwamuro, S. Miwa, T. Minowa, T. Enoki, X. F. Zhang et al., Activation of two types of Ca 2+-permeable nonselective cation channel by endothelin-1 in A7r5 cells, Br. J. Pharmacol, vol.124, pp.1541-1549, 1998.

M. Amaro, F. Reina, M. Hof, C. Eggeling, and E. Sezgin, Laurdan and Di-4-ANEPPDHQ probe different properties of the membrane, J. Phys. D Appl. Phys, vol.50, 2017.

A. I. Totlandsdal, F. R. Cassee, P. Schwarze, M. Refsnes, and M. Lag, Diesel exhaust particles induce CYP1A1 and pro-inflammatory responses via differential pathways in human bronchial epithelial cells, Part. Fibre Toxicol, vol.7, p.41, 2010.

Z. Andrysik, J. Vondracek, S. Marvanova, M. Ciganek, J. Neca et al., Activation of the aryl hydrocarbon receptor is the major toxic mode of action of an organic extract of a reference urban dust particulate matter mixture: The role of polycyclic aromatic hydrocarbons, Mutat. Res, vol.714, pp.53-62, 2011.

D. Y. Liu, A. Scholze, R. Kreutz, M. Wehland-von-trebra, W. Zidek et al., Monocytes from spontaneously hypertensive rats show increased store-operated and second messenger-operated calcium influx mediated by transient receptor potential canonical Type 3 channels, Am. J. Hypertens, vol.20, pp.1111-1118, 2007.

D. Y. Liu, F. Thilo, A. Scholze, A. Wittstock, Z. G. Zhao et al., Increased store-operated and 1-oleoyl-2-acetyl-sn-glycerol-induced calcium influx in monocytes is mediated by transient receptor potential canonical channels in human essential hypertension, J. Hypertens, vol.25, pp.799-808, 2007.

R. M. Krishnan, S. D. Adar, A. A. Szpiro, N. W. Jorgensen, V. C. Van-hee et al., Vascular responses to long-and short-term exposure to fine particulate matter: MESA Air (Multi-Ethnic Study of Atherosclerosis and Air Pollution), J. Am. Coll. Cardiol, vol.60, pp.2158-2166, 2012.

A. J. Lucking, M. Lundback, S. L. Barath, N. L. Mills, M. K. Sidhu et al., Particle traps prevent adverse vascular and prothrombotic effects of diesel engine exhaust inhalation in men, Circulation, vol.123, pp.1721-1728, 2011.

M. N'diaye, E. Le-ferrec, D. Lagadic-gossmann, S. Corre, D. Gilot et al., Aryl hydrocarbon receptor-and calcium-dependent induction of the chemokine CCL1 by the environmental contaminant benzo[a]pyrene, J. Biol. Chem, vol.281, 2006.

P. Monteiro, D. Gilot, E. Le-ferrec, C. Rauch, D. Lagadic-gossmann et al., Dioxin-mediated up-regulation of aryl hydrocarbon receptor target genes is dependent on the calcium/calmodulin/CaMKIalpha pathway, Mol. Pharmacol, vol.73, pp.769-777, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00696176

K. Dharmashankar and M. E. Widlansky, Vascular endothelial function and hypertension: Insights and directions, Curr. Hypertens. Rep, vol.12, pp.448-455, 2010.
DOI : 10.1007/s11906-010-0150-2

URL : http://europepmc.org/articles/pmc2982873?pdf=render

B. C. Brinchmann, E. L. Ferrec, N. Podechard, D. Lagadic-gossmann, J. A. Holme et al., Organic chemicals from diesel exhaust particles affects intracellular calcium, inflammation and ?-adrenoceptors in endothelial cells, Toxicol. Lett, 2018.

J. A. Araujo and A. E. Nel, Particulate matter and atherosclerosis: Role of particle size, composition and oxidative stress, Part. Fibre Toxicol, vol.6, 2009.
DOI : 10.1186/1743-8977-6-24

URL : https://particleandfibretoxicology.biomedcentral.com/track/pdf/10.1186/1743-8977-6-24?site=particleandfibretoxicology.biomedcentral.com

S. G. Klein, S. Cambier, J. Hennen, S. Legay, T. Serchi et al., Endothelial responses of the alveolar barrier in vitro in a dose-controlled exposure to diesel exhaust particulate matter, Part. Fibre Toxicol, vol.14, issue.7, 2017.

M. R. Miller, J. B. Raftis, J. P. Langrish, S. G. Mclean, P. Samutrtai et al., Inhaled Nanoparticles Accumulate at Sites of Vascular Disease, ACS Nano, vol.11, pp.4542-4552, 2017.

M. R. Miller, J. B. Raftis, J. P. Langrish, S. G. Mclean, P. Samutrtai et al., Inhaled Nanoparticles Accumulate at Sites of Vascular Disease, ACS Nano, vol.11, pp.10623-10624, 2017.

A. I. Totlandsdal, J. Ovrevik, R. E. Cochran, J. I. Herseth, A. K. Bolling et al., The occurrence of polycyclic aromatic hydrocarbons and their derivatives and the proinflammatory potential of fractionated extracts of diesel exhaust and wood smoke particles, J. Environ. Sci. Health A Tox. Hazard. Subst. Environ. Eng, vol.49, pp.383-396, 2014.

A. Kubátová, T. J. Lahren, J. Beránek, I. P. Smoliakova, A. Braun et al., Extractable Organic Carbon and its Differentiation by Polarity in Diesel Exhaust, Wood Smoke, and Urban Particulate Matter, Aerosol. Sci. Technol, vol.43, pp.714-729, 2009.

T. Stevens, S. H. Cho, W. P. Linak, and M. I. Gilmour, Differential potentiation of allergic lung disease in mice exposed to chemically distinct diesel samples, Toxicol. Sci, vol.107, pp.522-534, 2009.

J. A. Araujo, B. Barajas, M. Kleinman, X. Wang, B. J. Bennett et al., Ambient particulate pollutants in the ultrafine range promote early atherosclerosis and systemic oxidative stress, Circ. Res, vol.102, pp.589-596, 2008.

R. E. Cochran and A. Kubátová, Pressurised fluid extraction of polycyclic aromatic hydrocarbons and their polar oxidation products from atmospheric particles, Int. J. Environ. Anal. Chem, vol.95, pp.434-452, 2015.
DOI : 10.1080/03067319.2015.1025225

B. Zhao, D. E. Degroot, A. Hayashi, G. He, and M. Denison, CH223191 is a ligand-selective antagonist of the Ah (Dioxin) receptor, Toxicol. Sci, vol.117, pp.393-403, 2010.

W. Sun, K. Uchida, N. Takahashi, Y. Iwata, S. Wakabayashi et al., Activation of TRPV2 negatively regulates the differentiation of mouse brown adipocytes, Pflugers Arch. Eur. J. Physiol, vol.468, pp.1527-1540, 2016.

M. Law, J. L. Morales, L. F. Mottram, A. Iyer, B. R. Peterson et al., Structural requirements for the inhibition of calcium mobilization and mast cell activation by the pyrazole derivative BTP2, Int. J. Biochem. Cell Biol, vol.43, pp.1228-1239, 2011.

A. Mayati, N. Levoin, H. Paris, M. ;-n'diaye, A. Courtois et al., Induction of intracellular calcium concentration by environmental benzo(a)pyrene involves a ?2-adrenergic receptor/adenylyl cyclase/Epac-1/inositol 1,4,5-trisphosphate pathway in endothelial cells, J. Biol. Chem, vol.287, pp.4041-4052, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00682497

D. M. Owen, C. Rentero, A. Magenau, A. Abu-siniyeh, and K. Gaus, Quantitative imaging of membrane lipid order in cells and organisms, Nat. Protoc, vol.7, pp.24-35, 2011.