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scRNA-seq analysis discovered suppression of immunomodulatory dependent inflammatory response in PMBCs exposed to silver nanoparticles
by
Yoon, Tae-Hyun
, Perumalsamy, Haribalan
, Xiao, Xiao
, Kim, Hyun-Yi
in
AgNPs
/ Approximation
/ Biocompatibility
/ Biomedical materials
/ Biotechnology
/ CD16 antigen
/ Cell differentiation
/ Cell proliferation
/ Cells
/ Cellular-metal ion association
/ Chemistry
/ Chemistry and Materials Science
/ Cytokines
/ Cytotoxicity
/ Datasets
/ Depth profiling
/ Differentiation (biology)
/ Down-regulation
/ Gene expression
/ Genes
/ Genomics
/ Health aspects
/ Immune response
/ Immunology
/ Immunomodulation
/ Immunomodulators
/ Inflammation
/ Inflammatory response
/ Ion association
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Medical research
/ Medicine, Experimental
/ Metal ions
/ Metal Nanoparticles
/ Metallothionein
/ Metallothionein - genetics
/ Molecular Medicine
/ Monocytes
/ Monocytes - metabolism
/ Nanoparticles
/ Nanotechnology
/ Ontology
/ Particle size
/ Quality control
/ RNA sequencing
/ scRNA-seq analysis
/ Silver
/ Silver - pharmacology
/ Single-Cell Gene Expression Analysis
/ Toxicity
/ Up-regulation
/ Visualization
2024
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scRNA-seq analysis discovered suppression of immunomodulatory dependent inflammatory response in PMBCs exposed to silver nanoparticles
by
Yoon, Tae-Hyun
, Perumalsamy, Haribalan
, Xiao, Xiao
, Kim, Hyun-Yi
in
AgNPs
/ Approximation
/ Biocompatibility
/ Biomedical materials
/ Biotechnology
/ CD16 antigen
/ Cell differentiation
/ Cell proliferation
/ Cells
/ Cellular-metal ion association
/ Chemistry
/ Chemistry and Materials Science
/ Cytokines
/ Cytotoxicity
/ Datasets
/ Depth profiling
/ Differentiation (biology)
/ Down-regulation
/ Gene expression
/ Genes
/ Genomics
/ Health aspects
/ Immune response
/ Immunology
/ Immunomodulation
/ Immunomodulators
/ Inflammation
/ Inflammatory response
/ Ion association
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Medical research
/ Medicine, Experimental
/ Metal ions
/ Metal Nanoparticles
/ Metallothionein
/ Metallothionein - genetics
/ Molecular Medicine
/ Monocytes
/ Monocytes - metabolism
/ Nanoparticles
/ Nanotechnology
/ Ontology
/ Particle size
/ Quality control
/ RNA sequencing
/ scRNA-seq analysis
/ Silver
/ Silver - pharmacology
/ Single-Cell Gene Expression Analysis
/ Toxicity
/ Up-regulation
/ Visualization
2024
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scRNA-seq analysis discovered suppression of immunomodulatory dependent inflammatory response in PMBCs exposed to silver nanoparticles
by
Yoon, Tae-Hyun
, Perumalsamy, Haribalan
, Xiao, Xiao
, Kim, Hyun-Yi
in
AgNPs
/ Approximation
/ Biocompatibility
/ Biomedical materials
/ Biotechnology
/ CD16 antigen
/ Cell differentiation
/ Cell proliferation
/ Cells
/ Cellular-metal ion association
/ Chemistry
/ Chemistry and Materials Science
/ Cytokines
/ Cytotoxicity
/ Datasets
/ Depth profiling
/ Differentiation (biology)
/ Down-regulation
/ Gene expression
/ Genes
/ Genomics
/ Health aspects
/ Immune response
/ Immunology
/ Immunomodulation
/ Immunomodulators
/ Inflammation
/ Inflammatory response
/ Ion association
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Medical research
/ Medicine, Experimental
/ Metal ions
/ Metal Nanoparticles
/ Metallothionein
/ Metallothionein - genetics
/ Molecular Medicine
/ Monocytes
/ Monocytes - metabolism
/ Nanoparticles
/ Nanotechnology
/ Ontology
/ Particle size
/ Quality control
/ RNA sequencing
/ scRNA-seq analysis
/ Silver
/ Silver - pharmacology
/ Single-Cell Gene Expression Analysis
/ Toxicity
/ Up-regulation
/ Visualization
2024
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scRNA-seq analysis discovered suppression of immunomodulatory dependent inflammatory response in PMBCs exposed to silver nanoparticles
Journal Article
scRNA-seq analysis discovered suppression of immunomodulatory dependent inflammatory response in PMBCs exposed to silver nanoparticles
2024
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Overview
The assessment of AgNPs toxicity in vitro and in vivo models are frequently conflicting and inaccurate. Nevertheless, single cell immunological responses in a heterogenous environment have received little attention. Therefore, in this study, we have performed in-depth analysis which clearly revealed cellular-metal ion association as well as specific immunological response. Our study didn’t show significant population differences in PMBC between control and AgNPs group implying no toxicological response. To confirm it further, deep profiling identified differences in subsets and differentially expressed genes (DEGs) of monocytes, B cells and T cells. Notably, monocyte subsets showed significant upregulation of metallothionein (MT) gene expression such as
MT1G
,
MT1X
,
MT1E
,
MT1A
, and
MT1F.
On the other hand, downregulation of pro-inflammatory genes such as
IL1β
and
CCL3
in both CD16 + and CD16- monocyte subsets were observed. This result indicated that AgNPs association with monocyte subsets de-promoted inflammatory responsive genes suggesting no significant toxicity observed in AgNPs treated group. Other cell types such as B cells and T cells also showed negligible differences in their subsets suggesting no toxicity response. Further, AgNPs treated group showed upregulation of cell proliferation, ribosomal synthesis, downregulation of cytokine release, and T cell differentiation inhibition. Overall, our results conclude that treatment of AgNPs to PMBC cells didn’t display immunological related cytotoxicity response and thus motivate researchers to use them actively for biomedical applications.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
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