Cell source determines the immunological impact of biomimetic nanoparticles

Autor: Jonathan O. Martinez, Brandon S. Brown, Xuewu Liu, Nima Taghipour, Michael Evangelopoulos, Iman K. Yazdi, Nicoletta Quattrocchi, Christian Boada, Anne L. van de Ven, Ennio Tasciotti, Shilpa Scaria, Mauro Ferrari, Claudia Corbo, Alessandro Parodi, Armando Cevenini
Přispěvatelé: Evangelopoulos, Michael, Parodi, Alessandro, Martinez, Jonathan O., Yazdi, Iman K., Cevenini, Armando, van de Ven, Anne L., Quattrocchi, Nicoletta, Boada, Christian, Taghipour, Nima, Corbo, Claudia, Brown, Brandon S., Scaria, Shilpa, Liu, Xuewu, Ferrari, Mauro, Tasciotti, Ennio, Evangelopoulos, M, Parodi, A, Martinez, J, Yazdi, I, Cevenini, A, van de Ven, A, Quattrocchi, N, Boada, C, Taghipour, N, Corbo, C, Brown, B, Scaria, S, Liu, X, Ferrari, M, Tasciotti, E
Jazyk: angličtina
Předmět:
opsonization
leukocyte membrane
Cell
Biocompatible Materials
animal cell
02 engineering and technology
reactive oxygen metabolite
Mice
Nanoparticle
aspartate aminotransferase
Biomimetic Materials
drug delivery system
Macrophage
cell interaction
Leukolike Vector
comparative study
Cells
Cultured

tumor necrosis factor alpha
Systemic administration
creatinine
biomimetic material
Cell biology
Antibody opsonization
cytokine release
priority journal
nanocarrier
0210 nano-technology
surface charge
in vitro study
Biocompatibility
Biophysics
Ceramics and Composite
Bioengineering
macrophage
Article
animal tissue
in vivo study
Biomaterials
zeta potential
03 medical and health sciences
Nanovector
human
protein expression
mouse
human cell
Drug products
Biological materials
mononuclear phagocyte
Immunity
Innate

Cell membranes
030104 developmental biology
Immunology
interleukin 1alpha
Nanoparticles
Comprehensive evaluation
0301 basic medicine
interleukin 1beta
immunology
Bagg albino mouse
Biomimetics
Leukocytes
nanocapsule
animal
Multistage nanovector
innate immunity
Immunological effects
Mice
Inbred BALB C

Time-lapse microscopy
phagocytosis
021001 nanoscience & nanotechnology
unclassified drug
medicine.anatomical_structure
liver function
Mechanics of Materials
Drug delivery
gamma interferon
medicine.symptom
leukocyte
time lapse imaging
alanine aminotransferase
Antigen-antibody reactions
animal experiment
transcription factor RelA
interleukin 6
Inflammation
Biology
interleukin 2
Nanocapsules
interleukin 3
evaluation study
medicine
Biomimicry
Animals
controlled study
Mechanics of Material
Immunobiology
cell culture
nonhuman
static electricity
Biomaterial
Biomimetic nanoparticles
internalization
7 INGENIERÍA Y TECNOLOGÍA
drug effects
Ceramics and Composites
interleukin 12
interleukin 10
Zdroj: Biomaterials
ISSN: 0142-9612
DOI: 10.1016/j.biomaterials.2015.11.054
Popis: Recently, engineering the surface of nanotherapeutics with biologics to provide them with superior biocompatibility and targeting towards pathological tissues has gained significant popularity. Although the functionalization of drug delivery vectors with cellular materials has been shown to provide synthetic particles with unique biological properties, these approaches may have undesirable immunological repercussions upon systemic administration. Herein, we comparatively analyzed unmodified multistage nanovectors and particles functionalized with murine and human leukocyte cellular membrane, dubbed Leukolike Vectors (LLV), and the immunological effects that may arise in vitro and in vivo. Previously, LLV demonstrated an avoidance of opsonization and phagocytosis, in addition to superior targeting of inflammation and prolonged circulation. In this work, we performed a comprehensive evaluation of the importance of the source of cellular membrane in increasing their systemic tolerance and minimizing an inflammatory response. Time-lapse microscopy revealed LLV developed using a cellular coating derived from a murine (i.e., syngeneic) source resulted in an active avoidance of uptake by macrophage cells. Additionally, LLV composed of a murine membrane were found to have decreased uptake in the liver with no significant effect on hepatic function. As biomimicry continues to develop, this work demonstrates the necessity to consider the source of biological material in the development of future drug delivery carriers. © 2015.
Databáze: OpenAIRE