primary fibroblast cell cultures Search Results


90
Celprogen Inc synovial fluid membrane fibroblast primary cell culture complete media with serum
Synovial Fluid Membrane Fibroblast Primary Cell Culture Complete Media With Serum, supplied by Celprogen Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC primary human uterine fibroblast normal cells huf
Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine <t>fibroblast</t> cells <t>(HUF)</t> and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).
Primary Human Uterine Fibroblast Normal Cells Huf, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+fibroblast+cell+cultures/Primary+Uterine+Fibroblast+Cells%3B+Normal%2C+Human/pmc08160977-180-0-11
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ATCC cells normal human fibroblasts
Figure 1. Effects of specific wavelengths on the ability of IL-1α to stimulate matrix-related mRNA in fibroblasts. Human cultured fibroblasts were irradiated with 30 mJ of UVB, 5 J of UVA, 5 J of UVA1, or sham irradiated, and then given media without (minus symbols) or with (plus symbols) 10 ng IL-1α per ml, followed by 24 h of incubation at 37°C. Displayed are normalized levels of tropoelastin (A) and collagenase (B) mRNA.
Cells Normal Human Fibroblasts, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cells normal human fibroblasts - by Bioz Stars, 2026-09
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ATCC human lung fibroblast cells
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
Human Lung Fibroblast Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+fibroblast+cell+cultures/Primary+Lung+Fibroblast+Cells%3BFibrosis%2CHuman/10__1074_slash_jbc__m116__754622-184-2-9
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Cell Applications Inc t 75 flasks
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
T 75 Flasks, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+fibroblast+cell+cultures/Major+Media/bio_rxiv__64898__2026__04__03__716316-186-4-10
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93
ATCC human uterine fibroblast cells
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
Human Uterine Fibroblast Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+fibroblast+cell+cultures/Primary+Uterine%3B+Fibroblast+Cells%3B+Normal%2C+Human/pmc05933196-105-67-79
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Celprogen Inc human fibroblast nhf cell line
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
Human Fibroblast Nhf Cell Line, supplied by Celprogen Inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+fibroblast+cell+cultures/Human+Fibroblast+Primary+Cell+Culture/10__26554_slash_sti__2024__9__3__718___725-49-2-13
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Celprogen Inc mouse fibroblast cell culture complete medium
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
Mouse Fibroblast Cell Culture Complete Medium, supplied by Celprogen Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Celprogen Inc 36069 02 san pedro
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
36069 02 San Pedro, supplied by Celprogen Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+fibroblast+cell+cultures/Human+Synovial+Fluid+Normal+Membrane+Fibroblast+Cell+Culture+Frozen+Vials/pmc05983692-122-9-8
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CELLnTEC Advanced Cell Systems AG pooled human dermal fibroblasts hdfp
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
Pooled Human Dermal Fibroblasts Hdfp, supplied by CELLnTEC Advanced Cell Systems AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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European Collection of Authenticated Cell Cultures mrc-5 cells
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
Mrc 5 Cells, supplied by European Collection of Authenticated Cell Cultures, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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European Collection of Authenticated Cell Cultures cell line 1br3
FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 <t>fibroblasts.</t> WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).
Cell Line 1br3, supplied by European Collection of Authenticated Cell Cultures, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+fibroblast+cell+cultures/human+skin+normal+fibroblast+cell+line+1br+3+gn/pmc11430126-74-1-7
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Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine fibroblast cells (HUF) and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).

Journal: Nutrients

Article Title: Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein

doi: 10.3390/nu13051719

Figure Lengend Snippet: Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine fibroblast cells (HUF) and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).

Article Snippet: Primary human uterine fibroblast normal cells (HUF) were obtained from the ATCC.

Techniques: Derivative Assay, MTT Assay, Control, Standard Deviation, Concentration Assay

Figure 1. Effects of specific wavelengths on the ability of IL-1α to stimulate matrix-related mRNA in fibroblasts. Human cultured fibroblasts were irradiated with 30 mJ of UVB, 5 J of UVA, 5 J of UVA1, or sham irradiated, and then given media without (minus symbols) or with (plus symbols) 10 ng IL-1α per ml, followed by 24 h of incubation at 37°C. Displayed are normalized levels of tropoelastin (A) and collagenase (B) mRNA.

Journal: The Journal of investigative dermatology

Article Title: Wavelength-specific synergy between ultraviolet radiation and interleukin-1 alpha in the regulation of matrix-related genes: mechanistic role for tumor necrosis factor-alpha.

doi: 10.1046/j.1523-1747.1999.00681.x

Figure Lengend Snippet: Figure 1. Effects of specific wavelengths on the ability of IL-1α to stimulate matrix-related mRNA in fibroblasts. Human cultured fibroblasts were irradiated with 30 mJ of UVB, 5 J of UVA, 5 J of UVA1, or sham irradiated, and then given media without (minus symbols) or with (plus symbols) 10 ng IL-1α per ml, followed by 24 h of incubation at 37°C. Displayed are normalized levels of tropoelastin (A) and collagenase (B) mRNA.

Article Snippet: Cultured cells Normal human fibroblasts were obtained from the American Type Culture Collection (ATCC, Rockville, MD, catalog no. 1828X-CRL) and grown in Dulbecco’s modified Eagle’s medium supplemented with 10% fetal bovine serum.

Techniques: Cell Culture, Irradiation, Incubation

Figure 2. Effects of specific wavelengths on cellular secretion of TNF-α. (a) Fibroblasts were irradiated with 30 mJ of UVB, 5 J of UVA, 5 J of UVA1, or sham irradiated, and then given media without (minus symbols) or with (plus symbols) 10 ng IL-1α per ml, followed by 24 h of incubation at 37°C. Displayed are TNF-α concentrations in the conditioned media (n 5 2). (b) Keratinocytes were similarly irradiated, incubated, and media assayed for TNF-α. Displayed are TNF-α concentrations in the conditioned media when no exogenous IL-1α had been added (n 5 2). Separate experiments demonstrated that exogenous IL-1α did not affect secretion of TNF-α by keratinocytes exposed to any of these wavelengths. (c) Neonatal and adult keratinocytes were irradiated with 10 or 30 mJ per cm2 of UVB or 5 or 20 J per cm2 of UVA. Displayed are TNF-α concentrations in the conditioned media from irradiated neonatal (n 5 2) and adult (n 5 3) keratinocytes, p , 0.01 for adult 30 mJ per cm2 UVB relative to sham by analysis of variance, then Dunnett q9 statistic.

Journal: The Journal of investigative dermatology

Article Title: Wavelength-specific synergy between ultraviolet radiation and interleukin-1 alpha in the regulation of matrix-related genes: mechanistic role for tumor necrosis factor-alpha.

doi: 10.1046/j.1523-1747.1999.00681.x

Figure Lengend Snippet: Figure 2. Effects of specific wavelengths on cellular secretion of TNF-α. (a) Fibroblasts were irradiated with 30 mJ of UVB, 5 J of UVA, 5 J of UVA1, or sham irradiated, and then given media without (minus symbols) or with (plus symbols) 10 ng IL-1α per ml, followed by 24 h of incubation at 37°C. Displayed are TNF-α concentrations in the conditioned media (n 5 2). (b) Keratinocytes were similarly irradiated, incubated, and media assayed for TNF-α. Displayed are TNF-α concentrations in the conditioned media when no exogenous IL-1α had been added (n 5 2). Separate experiments demonstrated that exogenous IL-1α did not affect secretion of TNF-α by keratinocytes exposed to any of these wavelengths. (c) Neonatal and adult keratinocytes were irradiated with 10 or 30 mJ per cm2 of UVB or 5 or 20 J per cm2 of UVA. Displayed are TNF-α concentrations in the conditioned media from irradiated neonatal (n 5 2) and adult (n 5 3) keratinocytes, p , 0.01 for adult 30 mJ per cm2 UVB relative to sham by analysis of variance, then Dunnett q9 statistic.

Article Snippet: Cultured cells Normal human fibroblasts were obtained from the American Type Culture Collection (ATCC, Rockville, MD, catalog no. 1828X-CRL) and grown in Dulbecco’s modified Eagle’s medium supplemented with 10% fetal bovine serum.

Techniques: Irradiation, Incubation

Figure 3. Effects of exogenous TNF-α on the ability of IL-1α to stimulate tropoelastin mRNA in fibroblasts. Human cultured fibroblasts were incubated with or without IL-1α and TNF-α, as indicated. Displayed are normalized tropoelastin mRNA levels after 24 h of incubation at 37°C. IL-1α produced a statistically significant increase in tropoelastin mRNA only in the cells that received no TNF-α (p , 0.01 by t test).

Journal: The Journal of investigative dermatology

Article Title: Wavelength-specific synergy between ultraviolet radiation and interleukin-1 alpha in the regulation of matrix-related genes: mechanistic role for tumor necrosis factor-alpha.

doi: 10.1046/j.1523-1747.1999.00681.x

Figure Lengend Snippet: Figure 3. Effects of exogenous TNF-α on the ability of IL-1α to stimulate tropoelastin mRNA in fibroblasts. Human cultured fibroblasts were incubated with or without IL-1α and TNF-α, as indicated. Displayed are normalized tropoelastin mRNA levels after 24 h of incubation at 37°C. IL-1α produced a statistically significant increase in tropoelastin mRNA only in the cells that received no TNF-α (p , 0.01 by t test).

Article Snippet: Cultured cells Normal human fibroblasts were obtained from the American Type Culture Collection (ATCC, Rockville, MD, catalog no. 1828X-CRL) and grown in Dulbecco’s modified Eagle’s medium supplemented with 10% fetal bovine serum.

Techniques: Cell Culture, Incubation, Produced

Figure 4. Effect of anti-TNF-α antibodies on the ability of UVB to block the effect of IL-1α on matrix-related messages. Human cultured fibroblasts were irradiated with 30 mJ of UVB or sham irradiation, and then given media without (minus symbols) or with (plus symbols) 10 ng IL-1α per ml, plus the indicated concentrations of anti-TNF-α inhibitory antibodies. Displayed are normalized tropoelastin (a) and collagen (b) mRNA levels after 24 h of incubation at 37°C.

Journal: The Journal of investigative dermatology

Article Title: Wavelength-specific synergy between ultraviolet radiation and interleukin-1 alpha in the regulation of matrix-related genes: mechanistic role for tumor necrosis factor-alpha.

doi: 10.1046/j.1523-1747.1999.00681.x

Figure Lengend Snippet: Figure 4. Effect of anti-TNF-α antibodies on the ability of UVB to block the effect of IL-1α on matrix-related messages. Human cultured fibroblasts were irradiated with 30 mJ of UVB or sham irradiation, and then given media without (minus symbols) or with (plus symbols) 10 ng IL-1α per ml, plus the indicated concentrations of anti-TNF-α inhibitory antibodies. Displayed are normalized tropoelastin (a) and collagen (b) mRNA levels after 24 h of incubation at 37°C.

Article Snippet: Cultured cells Normal human fibroblasts were obtained from the American Type Culture Collection (ATCC, Rockville, MD, catalog no. 1828X-CRL) and grown in Dulbecco’s modified Eagle’s medium supplemented with 10% fetal bovine serum.

Techniques: Blocking Assay, Cell Culture, Irradiation, Incubation

FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 fibroblasts. WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).

Journal: Journal of Biological Chemistry

Article Title: Evidence That Factor VIII Forms a Bivalent Complex with the Low Density Lipoprotein (LDL) Receptor-related Protein 1 (LRP1)

doi: 10.1074/jbc.m116.754622

Figure Lengend Snippet: FIGURE 7. Effect of clusters II and IV on LRP1-mediated internalization of BDD-fVIII (A) and tPAPAI-1 (B) by WI-38 fibroblasts. WI-38 fibroblasts were seeded in 12-well tissue culture dishes (1 105 cells/well) and incubated with 20 nM 125I-BDD-fVIII (A) or 10 nM 125I-tPAPAI-1 (B) for 4 h at 37 °C in the presence orabsenceofLRP1clusterIIorIV(500nM).Followingincubation,theamountofradiolabeledligandinternalizedwasdetermined,andthedatawerenormalized to the amount of fVIII internalized in the absence of competitors. The results represent the mean of three independent experiments. Error bars represent S.E. (*, p 0.002, one-way analysis of variance with Tukey’s multiple comparison post-test).

Article Snippet: WI38 cells, human lung fibroblast cells, were obtained from American Type Culture Collection (ATCC) and maintained in DMEM (Corning) supplemented with 10% FBS and penicillin/streptomycin.

Techniques: Incubation, Comparison