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adult retinal pigment epithelial cell line arpe 19 (ATCC)

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ATCC adult retinal pigment epithelial cell line arpe 19

DIDS blocks binding and entry into multiple cell types permissive for HCMV infection. ( A – C ) HFFs ( A <t>),</t> <t>ARPE-19</t> ( B ) or U373 ( C ) cells were incubated with DIDS, NPPB, DMSO or media for 1h and then infected with HCMV and stained for IE gene expression 24 hpi, and infection was scored relative to DMSO control. ( D , E ) HFFs, ARPE-19 or U373 cells were pre-incubated with DIDS, DMSO, media and then infected with HCMV either at 37 °C ( D ) or 4 °C ( E ), and DNA was harvested 1 hpi and analyzed by qPCR and DNA expressed relative to DMSO control. n = 3 and error bars represent 1 standard deviation from the mean.

Adult Retinal Pigment Epithelial Cell Line Arpe 19, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 4465 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/retinal+pigment+epithelial+cell+line+arpe+19/ARPE-19/pmc13210247-34-0-25
Average 99 stars, based on 4465 article reviews

adult retinal pigment epithelial cell line arpe 19 - by Bioz Stars, 2026-09

99/100 stars

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1) Product Images from "A Potent Inhibitor of Human Cytomegalovirus Infection Works Post-Entry Specifically in Differentiating Myelo-Monocytic Cells"

Article Title: A Potent Inhibitor of Human Cytomegalovirus Infection Works Post-Entry Specifically in Differentiating Myelo-Monocytic Cells

Journal: Pathogens

doi: 10.3390/pathogens15050520

DIDS blocks binding and entry into multiple cell types permissive for HCMV infection. ( A – C ) HFFs ( A ), ARPE-19 ( B ) or U373 ( C ) cells were incubated with DIDS, NPPB, DMSO or media for 1h and then infected with HCMV and stained for IE gene expression 24 hpi, and infection was scored relative to DMSO control. ( D , E ) HFFs, ARPE-19 or U373 cells were pre-incubated with DIDS, DMSO, media and then infected with HCMV either at 37 °C ( D ) or 4 °C ( E ), and DNA was harvested 1 hpi and analyzed by qPCR and DNA expressed relative to DMSO control. n = 3 and error bars represent 1 standard deviation from the mean.

Figure Legend Snippet: DIDS blocks binding and entry into multiple cell types permissive for HCMV infection. ( A – C ) HFFs ( A ), ARPE-19 ( B ) or U373 ( C ) cells were incubated with DIDS, NPPB, DMSO or media for 1h and then infected with HCMV and stained for IE gene expression 24 hpi, and infection was scored relative to DMSO control. ( D , E ) HFFs, ARPE-19 or U373 cells were pre-incubated with DIDS, DMSO, media and then infected with HCMV either at 37 °C ( D ) or 4 °C ( E ), and DNA was harvested 1 hpi and analyzed by qPCR and DNA expressed relative to DMSO control. n = 3 and error bars represent 1 standard deviation from the mean.

Techniques Used: Binding Assay, Infection, Incubation, Staining, Gene Expression, Control, Standard Deviation

DIDS has cell type-specific differences in time of addition studies that correlate with gB antibody phenotypes. ( A ) HFFs or ARPE-19 cells were incubated with DIDS (50 uM) at intervals between 1 h pre-infection to 4 hpi with TB40/e and assessed for anti-viral activity against infection. Infection was scored by immunostaining for IE gene expression 24 hpi relative to the DMSO control. ( B ) HFFs or ARPE-19 cells were incubated with anti-gB neutralizing antibody ITC-88 (5 ug/mL), 1 h pre-infection to 1 hpi with HCMV. Infection was scored by immunostaining for IE gene expression 24 hpi relative to the IgG control. n = 3 and error bars represent 1 standard deviation from the mean. A two-way ANOVA analysis with multiple comparisons was performed. * p < 0.05.

Figure Legend Snippet: DIDS has cell type-specific differences in time of addition studies that correlate with gB antibody phenotypes. ( A ) HFFs or ARPE-19 cells were incubated with DIDS (50 uM) at intervals between 1 h pre-infection to 4 hpi with TB40/e and assessed for anti-viral activity against infection. Infection was scored by immunostaining for IE gene expression 24 hpi relative to the DMSO control. ( B ) HFFs or ARPE-19 cells were incubated with anti-gB neutralizing antibody ITC-88 (5 ug/mL), 1 h pre-infection to 1 hpi with HCMV. Infection was scored by immunostaining for IE gene expression 24 hpi relative to the IgG control. n = 3 and error bars represent 1 standard deviation from the mean. A two-way ANOVA analysis with multiple comparisons was performed. * p < 0.05.

Techniques Used: Incubation, Infection, Activity Assay, Immunostaining, Gene Expression, Control, Standard Deviation

DIDS reduces ISG induction by viral infection. ( A , B ) CD14+ monocytes were pre-treated with DIDS (50 uM) or DMSO and then infected with HCMV and analyzed for ISG expression at 6 and 24 hpi by qRT-PCR. All datasets are expressed relative to infected media control. n = 3 and error bars represent 1 standard deviation from the mean. Dashed line represents 1 (no change) For ( A , B ) Mann–Whitney U comparison of the means was performed. * p < 0.05; ** p < 0.01 ( C ) An array analysis for the expression of a panel of ISGs in response to viral infection of CD14+ monocytes, ARPE-19, HFFs and MoDCs was performed at 24 hpi in infected cells pre-treated with DIDS (50 uM) or DMSO control for 1 h. Data from a single experiment was analyzed in duplicate.

Figure Legend Snippet: DIDS reduces ISG induction by viral infection. ( A , B ) CD14+ monocytes were pre-treated with DIDS (50 uM) or DMSO and then infected with HCMV and analyzed for ISG expression at 6 and 24 hpi by qRT-PCR. All datasets are expressed relative to infected media control. n = 3 and error bars represent 1 standard deviation from the mean. Dashed line represents 1 (no change) For ( A , B ) Mann–Whitney U comparison of the means was performed. * p < 0.05; ** p < 0.01 ( C ) An array analysis for the expression of a panel of ISGs in response to viral infection of CD14+ monocytes, ARPE-19, HFFs and MoDCs was performed at 24 hpi in infected cells pre-treated with DIDS (50 uM) or DMSO control for 1 h. Data from a single experiment was analyzed in duplicate.

Techniques Used: Infection, Expressing, Quantitative RT-PCR, Control, Standard Deviation, MANN-WHITNEY, Comparison

other:

Article Title: Quercetin attenuates high glucose-induced VEGFA expression in ARPE-19 cells by inhibiting ROS generation, p38 MAPK phosphorylation, and NF-κB activation.
Article Snippet: This study used the human retinal pigment epithelial cell line ARPE-19 (ATCC CRL2302).

Article Title: Quercetin attenuates high glucose-induced VEGFA expression in ARPE-19 cells by inhibiting ROS generation, p38 MAPK phosphorylation, and NF-κB activation
Article Snippet: This study used the human retinal pigment epithelial cell line ARPE-19 (ATCC CRL-2302).

Cell Culture:

Article Title: Immunogenicity and plasmid delivery pathways of non-invasive Lactococcus lactis -vectored mucosal DNA vaccination.
Article Snippet: The murine colonic epithelial cell line CMT-93 (ATCC) was cultured in low-glucose Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% FBS at 37°C in 5% CO2. .. The human retinal pigment epithelial cell line ARPE-19 (ATCC) was cultured in high-glucose DMEM/Ham’s F-12 supplemented with 10% FBS at 37°C in 5% CO2. ..

Article Title: Immunogenicity and plasmid delivery pathways of non-invasive Lactococcus lactis -vectored mucosal DNA vaccination
Article Snippet: The murine colonic epithelial cell line CMT-93 (ATCC) was cultured in low-glucose Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% FBS at 37°C in 5% CO 2 . .. The human retinal pigment epithelial cell line ARPE-19 (ATCC) was cultured in high-glucose DMEM/Ham’s F-12 supplemented with 10% FBS at 37°C in 5% CO 2 . ..

Article Title: Retinal pigment epithelium drives macrophage migration during Toxoplasma gondii infection in vitro
Article Snippet: .. ARPE-19 cell culture - The immortalized human retinal pigment epithelial cell line ARPE-19 (ATCC CRL-2302) was kindly provided by the CASO Laboratory, Federal University of São Paulo, Brazil. .. Cells were maintained in Dulbecco’s Modified Eagle Medium/Nutrient Mixture F-12 (DMEM/F-12; Thermo Fisher Scientific) supplemented with 10% (v/v) heat-inactivated fetal bovine serum (FBS; Gibco), 100 U mL−1 penicillin and 100 μg mL−1 streptomycin, at 37oC in a humidified atmosphere containing 5% CO2, as previously described.

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Journal: Pathogens

Article Title: A Potent Inhibitor of Human Cytomegalovirus Infection Works Post-Entry Specifically in Differentiating Myelo-Monocytic Cells

doi: 10.3390/pathogens15050520

Figure Lengend Snippet: DIDS blocks binding and entry into multiple cell types permissive for HCMV infection. ( A – C ) HFFs ( A ), ARPE-19 ( B ) or U373 ( C ) cells were incubated with DIDS, NPPB, DMSO or media for 1h and then infected with HCMV and stained for IE gene expression 24 hpi, and infection was scored relative to DMSO control. ( D , E ) HFFs, ARPE-19 or U373 cells were pre-incubated with DIDS, DMSO, media and then infected with HCMV either at 37 °C ( D ) or 4 °C ( E ), and DNA was harvested 1 hpi and analyzed by qPCR and DNA expressed relative to DMSO control. n = 3 and error bars represent 1 standard deviation from the mean.

Article Snippet: Adult retinal pigment epithelial cell line ARPE-19 (CRL-2302), monocyte cell line THP-1 cells (TIB-202) and primary human fetal foreskin fibroblasts (HFFs, SCRC-1041) were purchased from ATCC.

Techniques: Binding Assay, Infection, Incubation, Staining, Gene Expression, Control, Standard Deviation

Journal: Pathogens

Article Title: A Potent Inhibitor of Human Cytomegalovirus Infection Works Post-Entry Specifically in Differentiating Myelo-Monocytic Cells

doi: 10.3390/pathogens15050520

Figure Lengend Snippet: DIDS has cell type-specific differences in time of addition studies that correlate with gB antibody phenotypes. ( A ) HFFs or ARPE-19 cells were incubated with DIDS (50 uM) at intervals between 1 h pre-infection to 4 hpi with TB40/e and assessed for anti-viral activity against infection. Infection was scored by immunostaining for IE gene expression 24 hpi relative to the DMSO control. ( B ) HFFs or ARPE-19 cells were incubated with anti-gB neutralizing antibody ITC-88 (5 ug/mL), 1 h pre-infection to 1 hpi with HCMV. Infection was scored by immunostaining for IE gene expression 24 hpi relative to the IgG control. n = 3 and error bars represent 1 standard deviation from the mean. A two-way ANOVA analysis with multiple comparisons was performed. * p < 0.05.

Techniques: Incubation, Infection, Activity Assay, Immunostaining, Gene Expression, Control, Standard Deviation

Journal: Pathogens

Article Title: A Potent Inhibitor of Human Cytomegalovirus Infection Works Post-Entry Specifically in Differentiating Myelo-Monocytic Cells

doi: 10.3390/pathogens15050520

Figure Lengend Snippet: DIDS reduces ISG induction by viral infection. ( A , B ) CD14+ monocytes were pre-treated with DIDS (50 uM) or DMSO and then infected with HCMV and analyzed for ISG expression at 6 and 24 hpi by qRT-PCR. All datasets are expressed relative to infected media control. n = 3 and error bars represent 1 standard deviation from the mean. Dashed line represents 1 (no change) For ( A , B ) Mann–Whitney U comparison of the means was performed. * p < 0.05; ** p < 0.01 ( C ) An array analysis for the expression of a panel of ISGs in response to viral infection of CD14+ monocytes, ARPE-19, HFFs and MoDCs was performed at 24 hpi in infected cells pre-treated with DIDS (50 uM) or DMSO control for 1 h. Data from a single experiment was analyzed in duplicate.

Techniques: Infection, Expressing, Quantitative RT-PCR, Control, Standard Deviation, MANN-WHITNEY, Comparison

transmembrane migration of adult retinal pigment epithelial (ARPE-19) cells through Transwell® insert pores to the lower surface of the membrane. (A, B) ARPE-19 cells showing gaps (arrows) corresponding to pores on the lower membrane surface without cell coverage. (C, D) Sensitised ARPE-19 cells (ARPE-19-S) forming a continuous monolayer completely covering the pores.

Journal: Memórias do Instituto Oswaldo Cruz

Article Title: Retinal pigment epithelium drives macrophage migration during Toxoplasma gondii infection in vitro

doi: 10.1590/0074-02760250141

Figure Lengend Snippet: transmembrane migration of adult retinal pigment epithelial (ARPE-19) cells through Transwell® insert pores to the lower surface of the membrane. (A, B) ARPE-19 cells showing gaps (arrows) corresponding to pores on the lower membrane surface without cell coverage. (C, D) Sensitised ARPE-19 cells (ARPE-19-S) forming a continuous monolayer completely covering the pores.

Article Snippet: ARPE-19 cell culture - The immortalized human retinal pigment epithelial cell line ARPE-19 (ATCC CRL-2302) was kindly provided by the CASO Laboratory, Federal University of São Paulo, Brazil.

Techniques: Migration, Membrane

Transwell® migration assay showing adult retinal pigment epithelial (ARPE-19) cell migration through membrane pores and adhesion to the lower surface of the well. (A) Control condition. (B) Exposure to Toxoplasma gondii RH strain (2.5 × 10⁻³ μg/μL). (C) Exposure to soluble T. gondii antigen. Both stimuli increased the migratory response.

Journal: Memórias do Instituto Oswaldo Cruz

Article Title: Retinal pigment epithelium drives macrophage migration during Toxoplasma gondii infection in vitro

doi: 10.1590/0074-02760250141

Figure Lengend Snippet: Transwell® migration assay showing adult retinal pigment epithelial (ARPE-19) cell migration through membrane pores and adhesion to the lower surface of the well. (A) Control condition. (B) Exposure to Toxoplasma gondii RH strain (2.5 × 10⁻³ μg/μL). (C) Exposure to soluble T. gondii antigen. Both stimuli increased the migratory response.

Techniques: Transwell Migration Assay, Migration, Membrane, Control

chemotaxis of adult retinal pigment epithelial (ARPE-19) and sensitised ARPE-19 cells in the under-agar assay after 24 h. Representative images under different experimental conditions. Arrows indicate the migration front.

Journal: Memórias do Instituto Oswaldo Cruz

Article Title: Retinal pigment epithelium drives macrophage migration during Toxoplasma gondii infection in vitro

doi: 10.1590/0074-02760250141

Figure Lengend Snippet: chemotaxis of adult retinal pigment epithelial (ARPE-19) and sensitised ARPE-19 cells in the under-agar assay after 24 h. Representative images under different experimental conditions. Arrows indicate the migration front.

Techniques: Chemotaxis Assay, Migration

quantification of adult retinal pigment epithelial (ARPE-19) cell migration in the Transwell® assay after exposure to different stimuli. Bars represent the number of cells in the lower chamber following exposure to live tachyzoites, conditioned supernatant or soluble antigen (0.12-2.0 μg). Values are mean ± standard deviation (SD) (n = 3). *p < 0.05 versus control [analysis of variance (ANOVA)/Tukey].

Journal: Memórias do Instituto Oswaldo Cruz

Article Title: Retinal pigment epithelium drives macrophage migration during Toxoplasma gondii infection in vitro

doi: 10.1590/0074-02760250141

Figure Lengend Snippet: quantification of adult retinal pigment epithelial (ARPE-19) cell migration in the Transwell® assay after exposure to different stimuli. Bars represent the number of cells in the lower chamber following exposure to live tachyzoites, conditioned supernatant or soluble antigen (0.12-2.0 μg). Values are mean ± standard deviation (SD) (n = 3). *p < 0.05 versus control [analysis of variance (ANOVA)/Tukey].

Techniques: Migration, Transwell Assay, Standard Deviation, Control

Preparation and characterization of the conjugates (A) Schematic diagram of responsive release of the conjugates. (B) Particle size and distribution of aVEGFA, MPEG-aVEGFA, and the conjugates. (C) Particle size changes of aVEGFA, MPEG-aVEGFA, and the conjugates after incubation in hydrogen peroxide. (D) Transmission electron microscopy images of aVEGFA and the conjugates, scale bar = 100 nm. (E–G) Schematic diagram and quantitative results of in vitro experiments assessing corneal penetration ability of FITC-aVEGFA. (H, I) Schematic diagram and quantitative results of in vitro experiments assessing corneal penetration ability of FITC-aPDL1. (J, K) Cytotoxicity evaluation of TAT-MPEG-aVEGFA on HCE-T cells and ARPE19 cells. (L, M) Scratch assay results estimating angiogenesis inhibition, and quantitative analysis. n.s. (not significant) p > 0.05, *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 versus control. Abbreviations: aVEGFA, anti–vascular endothelial growth factor A antibody; TAT-MPEG, trans-activator of transcription peptide–methoxy polyethylene glycol; ARPE-19, human retinal pigment epithelial cell line; HCE-T, human corneal epithelial cell line.

Journal: Materials Today Bio

Article Title: ROS-responsive transmembrane peptide-antibody conjugate eyedrops for the non-invasive treatment of choroidoretinopathy

doi: 10.1016/j.mtbio.2026.102819

Figure Lengend Snippet: Preparation and characterization of the conjugates (A) Schematic diagram of responsive release of the conjugates. (B) Particle size and distribution of aVEGFA, MPEG-aVEGFA, and the conjugates. (C) Particle size changes of aVEGFA, MPEG-aVEGFA, and the conjugates after incubation in hydrogen peroxide. (D) Transmission electron microscopy images of aVEGFA and the conjugates, scale bar = 100 nm. (E–G) Schematic diagram and quantitative results of in vitro experiments assessing corneal penetration ability of FITC-aVEGFA. (H, I) Schematic diagram and quantitative results of in vitro experiments assessing corneal penetration ability of FITC-aPDL1. (J, K) Cytotoxicity evaluation of TAT-MPEG-aVEGFA on HCE-T cells and ARPE19 cells. (L, M) Scratch assay results estimating angiogenesis inhibition, and quantitative analysis. n.s. (not significant) p > 0.05, *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 versus control. Abbreviations: aVEGFA, anti–vascular endothelial growth factor A antibody; TAT-MPEG, trans-activator of transcription peptide–methoxy polyethylene glycol; ARPE-19, human retinal pigment epithelial cell line; HCE-T, human corneal epithelial cell line.

Article Snippet: Murine melanoma (B16) cells were obtained from COBIOER Biotechnology (Nanjing, China), human retinal pigment epithelial cell line (ARPE-19) cells and human corneal epithelial cell line (HCE-T) cells were obtained from ProCell Biotechnology (Wuhan, China), HUVECs were obtained from SUNNCELL Biotechnology (Wuhan, China).

Techniques: Incubation, Transmission Assay, Electron Microscopy, In Vitro, Wound Healing Assay, Inhibition, Control

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adult retinal pigment epithelial cell line arpe 19 (ATCC)

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1) Product Images from "A Potent Inhibitor of Human Cytomegalovirus Infection Works Post-Entry Specifically in Differentiating Myelo-Monocytic Cells"

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