TY - JOUR
T1 - Zebrafish, a model to develop nanotherapeutics that control neutrophils response during inflammation
AU - García-López, Juan P.
AU - Vilos, Cristian
AU - Feijóo, Carmen G.
N1 - Funding Information:
JP.G. Acknowledges support from Doctoral scholarship REX 2380-2015 . C.G.F., and C.V., acknowledges the support from Nucleus-Unab DI-36-18 /“N”. Authors acknowledge support from CONICYT under FONDECYT #1171199 (CG.F.), #1161438 (C.V.), and BASAL Grant FB0807 . C.V., also, thanks to H2020-MSCA-RISE-2016 #734801 MAGNAMED . Appendix A
PY - 2019/11/10
Y1 - 2019/11/10
N2 - Neutrophils are crucial modulators of the inflammation process, and their uncontrolled response worsens several chronic pathologies. The p38 mitogen-activated protein kinases (MAPKs) activity is critical for normal immune and inflammatory response through the regulation of pro-inflammatory cytokines synthesis. In this work, we study the effect of hybrid lipid–polymer nanoparticles loaded with the p38 MAPK inhibitor SB203580 in an acute and chronic inflammatory model in zebrafish containing a transgenic neutrophil cell line that constitutively expresses a green fluorescent protein. We identify the existence of at least two neutrophils subpopulation involved in the response during the acute inflammation triggered; a first-responder p38α–independent subset and a second-responder p38α-dependent subset. In the case of chronic inflammation, neutrophils recruited in the intestine only during the inflammation process, migrate in a p38α-dependent manner. Likewise, we establish that SB203580–loaded in NPs exerts their action during at least a double period than the inhibitor administers directly in both types of inflammation. Our results demonstrate the exceptional potential of the zebrafish as an inflammatory model for studying novel nanotherapeutics that selectively inhibit the neutrophils response, and to identify functional neutrophils subpopulations involved in the inflammation process.
AB - Neutrophils are crucial modulators of the inflammation process, and their uncontrolled response worsens several chronic pathologies. The p38 mitogen-activated protein kinases (MAPKs) activity is critical for normal immune and inflammatory response through the regulation of pro-inflammatory cytokines synthesis. In this work, we study the effect of hybrid lipid–polymer nanoparticles loaded with the p38 MAPK inhibitor SB203580 in an acute and chronic inflammatory model in zebrafish containing a transgenic neutrophil cell line that constitutively expresses a green fluorescent protein. We identify the existence of at least two neutrophils subpopulation involved in the response during the acute inflammation triggered; a first-responder p38α–independent subset and a second-responder p38α-dependent subset. In the case of chronic inflammation, neutrophils recruited in the intestine only during the inflammation process, migrate in a p38α-dependent manner. Likewise, we establish that SB203580–loaded in NPs exerts their action during at least a double period than the inhibitor administers directly in both types of inflammation. Our results demonstrate the exceptional potential of the zebrafish as an inflammatory model for studying novel nanotherapeutics that selectively inhibit the neutrophils response, and to identify functional neutrophils subpopulations involved in the inflammation process.
KW - Acute & chronic inflammation
KW - Neutrophil recruitment
KW - p38 MAP Kinase
KW - Polymeric nanoparticles
KW - Zebrafish
UR - http://www.scopus.com/inward/record.url?scp=85073513840&partnerID=8YFLogxK
U2 - 10.1016/j.jconrel.2019.10.005
DO - 10.1016/j.jconrel.2019.10.005
M3 - Article
C2 - 31622693
AN - SCOPUS:85073513840
SN - 0168-3659
VL - 313
SP - 14
EP - 23
JO - Journal of Controlled Release
JF - Journal of Controlled Release
ER -