Review



murine embryonic fibroblast mef cell line  (ATCC)


Bioz Verified Symbol ATCC is a verified supplier
Bioz Manufacturer Symbol ATCC manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 95

    Structured Review

    ATCC murine embryonic fibroblast mef cell line
    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse <t>fibroblast</t> cells <t>(MEF),</t> and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Murine Embryonic Fibroblast Mef Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 563 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/murine+embryonic+fibroblast+mef+cell+line/MEF/pmc12859411-217-1-11
    Average 95 stars, based on 563 article reviews
    murine embryonic fibroblast mef cell line - by Bioz Stars, 2026-09
    95/100 stars

    Images

    1) Product Images from "Collagen depletion by pirfenidone enhances antitumor effect of oncolytic adenovirus against peritoneal metastases of gastric cancer"

    Article Title: Collagen depletion by pirfenidone enhances antitumor effect of oncolytic adenovirus against peritoneal metastases of gastric cancer

    Journal: Molecular Therapy Oncology

    doi: 10.1016/j.omton.2025.201045

    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse fibroblast cells (MEF), and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Figure Legend Snippet: GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse fibroblast cells (MEF), and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Techniques Used: Expressing, Quantitative RT-PCR, Incubation, Control, Staining, Software

    Collagens and fibroblasts inhibit oncolytic virus penetration and reduce antitumor effects (A) T3-2D, MKN45, MEF, and YS-1 cells were infected with OBP-702 at the indicated MOIs for 3 days. Cell viability was assessed using the XTT assays. Cell viability was calculated relative to that of the mock-infected cells, which were set as 1.0. Data are expressed as the mean ± SD ( n = 5). (B) T3-2D and MKN45 cells were infected with OBP-702 at the indicated MOIs for 3 days with or without 10% collagen containing medium. Cell viability was assessed using the XTT assays. Cell viability was calculated relative to that of the mock-infected cells, which were set as 1.0. Data are expressed as the mean ± SD ( n = 5). (C) Representative cellular morphological images of T3-2D and MKN45 cells infected with 100 MOI of OBP-702 with or without 10% collagen stimulation for 72 h. Scale bars, 100 μm. (D) Representative spheroid morphological images of T3-2D cells infected with 20 MOI of OBP-702 or MKN45 cells infected with 50 MOI of OBP-702 with or without 2% collagen stimulation for 7 days. Scale bars, 100 μm. (E) ATP cell viability assay of T3-2D and MKN45 spheroids with or without 2% collagen stimulation for 7 days after infection with OBP-702 (20 MOI or 50 MOI). Data are expressed as the mean ± SD ( n = 5). (F) Representative images of mono-spheroids and co-cultured spheroids infected with OBP-401 (100 MOI) for 48 h. T3-2D and MKN45 cells were labeled with red cell trackers and MEF and YS-1 cells with blue cell trackers. Scale bars, 50 μm. ∗∗ p < 0.01, ∗∗∗ p < 0.001.
    Figure Legend Snippet: Collagens and fibroblasts inhibit oncolytic virus penetration and reduce antitumor effects (A) T3-2D, MKN45, MEF, and YS-1 cells were infected with OBP-702 at the indicated MOIs for 3 days. Cell viability was assessed using the XTT assays. Cell viability was calculated relative to that of the mock-infected cells, which were set as 1.0. Data are expressed as the mean ± SD ( n = 5). (B) T3-2D and MKN45 cells were infected with OBP-702 at the indicated MOIs for 3 days with or without 10% collagen containing medium. Cell viability was assessed using the XTT assays. Cell viability was calculated relative to that of the mock-infected cells, which were set as 1.0. Data are expressed as the mean ± SD ( n = 5). (C) Representative cellular morphological images of T3-2D and MKN45 cells infected with 100 MOI of OBP-702 with or without 10% collagen stimulation for 72 h. Scale bars, 100 μm. (D) Representative spheroid morphological images of T3-2D cells infected with 20 MOI of OBP-702 or MKN45 cells infected with 50 MOI of OBP-702 with or without 2% collagen stimulation for 7 days. Scale bars, 100 μm. (E) ATP cell viability assay of T3-2D and MKN45 spheroids with or without 2% collagen stimulation for 7 days after infection with OBP-702 (20 MOI or 50 MOI). Data are expressed as the mean ± SD ( n = 5). (F) Representative images of mono-spheroids and co-cultured spheroids infected with OBP-401 (100 MOI) for 48 h. T3-2D and MKN45 cells were labeled with red cell trackers and MEF and YS-1 cells with blue cell trackers. Scale bars, 50 μm. ∗∗ p < 0.01, ∗∗∗ p < 0.001.

    Techniques Used: Virus, Infection, Viability Assay, Cell Culture, Labeling

    Related Articles

    Control:

    Article Title: Vitamin K 2 induces non-apoptotic cell death along with autophagosome formation in breast cancer cell lines.
    Article Snippet: Background Vitamin K2 (VK2) has been reported to induce apoptosis in many types of cancer cells including leukemia.. However, there are no precise reports regarding the breast cancer cells.. From the stand point of clinical implications of VK2 including chemoprevention, we investigated the effects of VK2 on breast cancer cell lines.

    Article Title: Targeting the integrated networks of aggresome formation, proteasome, and autophagy potentiates ER stress-mediated cell death in multiple myeloma cells
    Article Snippet: The human MM cell line KMS-12-PE was obtained from the Japanese Collection of Research Bioresources (JCRB) (Osaka, Japan). .. A CHOP −/− murine embryonic fibroblast (MEF) cell line (CHOP-KO-DR) established from a 13.5-day-old CHOP −/− mouse embryo by SV-40 immortalization and a CHOP +/+ MEF cell line (DR-wild-type) established by SV-40 immortalization as a control cell line for CHOP-KO-DR were also obtained from the ATCC. ..



    Similar Products

    95
    ATCC murine embryonic fibroblast mef cell line
    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse <t>fibroblast</t> cells <t>(MEF),</t> and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Murine Embryonic Fibroblast Mef Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/murine+embryonic+fibroblast+mef+cell+line/MEF/pmc12859411-217-1-11
    Average 95 stars, based on 1 article reviews
    murine embryonic fibroblast mef cell line - by Bioz Stars, 2026-09
    95/100 stars
      Buy from Supplier

    94
    ATCC 2993 murine embryonic fibroblasts cell line drg neuronal cells adult mouse dorsal root ganglion
    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse <t>fibroblast</t> cells <t>(MEF),</t> and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    2993 Murine Embryonic Fibroblasts Cell Line Drg Neuronal Cells Adult Mouse Dorsal Root Ganglion, 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/murine+embryonic+fibroblast+mef+cell+line/Mfn2-null+MEFs/10__7554_slash_elife__84235-272-134-132
    Average 94 stars, based on 1 article reviews
    2993 murine embryonic fibroblasts cell line drg neuronal cells adult mouse dorsal root ganglion - by Bioz Stars, 2026-09
    94/100 stars
      Buy from Supplier

    94
    ATCC murine embryonic fibroblast cell line crl
    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse <t>fibroblast</t> cells <t>(MEF),</t> and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Murine Embryonic Fibroblast Cell Line Crl, 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/murine+embryonic+fibroblast+mef+cell+line/WT+SV40+MEF/pmc09020777-420-32-29
    Average 94 stars, based on 1 article reviews
    murine embryonic fibroblast cell line crl - by Bioz Stars, 2026-09
    94/100 stars
      Buy from Supplier

    95
    ATCC murine embryonic fibroblast mef cell lines
    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse <t>fibroblast</t> cells <t>(MEF),</t> and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Murine Embryonic Fibroblast Mef Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/murine+embryonic+fibroblast+mef+cell+line/MEF/pm32365526-36-5-19
    Average 95 stars, based on 1 article reviews
    murine embryonic fibroblast mef cell lines - by Bioz Stars, 2026-09
    95/100 stars
      Buy from Supplier

    93
    ATCC crl 2992 murine embryonic fibroblasts cell line
    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse <t>fibroblast</t> cells <t>(MEF),</t> and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Crl 2992 Murine Embryonic Fibroblasts Cell Line, 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/murine+embryonic+fibroblast+mef+cell+line/Mfn1-null+MEFs/10__7554_slash_elife__61119-181-67-54
    Average 93 stars, based on 1 article reviews
    crl 2992 murine embryonic fibroblasts cell line - by Bioz Stars, 2026-09
    93/100 stars
      Buy from Supplier

    95
    ATCC mef murine embryonic fibroblasts cell lines
    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse <t>fibroblast</t> cells <t>(MEF),</t> and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Mef Murine Embryonic Fibroblasts Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/murine+embryonic+fibroblast+mef+cell+line/MEF/pmc06965651-40-62-71
    Average 95 stars, based on 1 article reviews
    mef murine embryonic fibroblasts cell lines - by Bioz Stars, 2026-09
    95/100 stars
      Buy from Supplier

    94
    Addgene inc hes cell line murine embryonic fibroblasts mefs
    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse <t>fibroblast</t> cells <t>(MEF),</t> and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Hes Cell Line Murine Embryonic Fibroblasts Mefs, supplied by Addgene inc, 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/murine+embryonic+fibroblast+mef+cell+line/pCas9_GFP+(Plasmid+%2344719)/pm30358158-131-2-14
    Average 94 stars, based on 1 article reviews
    hes cell line murine embryonic fibroblasts mefs - by Bioz Stars, 2026-09
    94/100 stars
      Buy from Supplier

    Image Search Results


    GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse fibroblast cells (MEF), and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Journal: Molecular Therapy Oncology

    Article Title: Collagen depletion by pirfenidone enhances antitumor effect of oncolytic adenovirus against peritoneal metastases of gastric cancer

    doi: 10.1016/j.omton.2025.201045

    Figure Lengend Snippet: GC cells increase collagen 1 expression in fibroblasts and collagen increases proliferation of GC cells (A) Expressions of Col1A1, Col1A2, and ACTA2 mRNA in mouse gastric cancer (GC) cells (T3-2D), human GC cells (MKN45, MKN7, and NUGC4), mouse fibroblast cells (MEF), and human fibroblast cells (YS-1 and FEF3) are shown. All cells were analyzed by quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (B) Expression of Col1A1 and Col1A2 mRNA in MEF (upper) and YS-1 (lower) cells after incubation with serum-free medium (SFM) as a control and conditioned medium (CM) of each GC cell type for 4 days. Cells were analyzed using quantitative RT-PCR analysis. Data are expressed as the mean ± SD ( n = 3). (C) Representative images of immunocytochemical staining of collagen 1 and α-SMA in MEF (left) and YS-1 (right) after incubation with normal medium and CM of each of the GC cells for 4 days. SFM was used as a control. The area index for each staining was evaluated by ImageJ software. Data are expressed as the mean ± SD ( n = 3). Scale bars, 50 μm. (D) Cell proliferation of T3-2D and MKN45 cells with and without 10% collagen stimulation for 72 h. Data are expressed as the mean ± SD ( n = 5). (E) Representative cellular morphological images of T3-2D and MKN45 cells with and without 10% collagen 1 stimulation for 72 h. Scale bar, 100 μm. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Article Snippet: A murine embryonic fibroblast (MEF) cell line was purchased from the American Type Culture Collection (Manassas, VA) and maintained in DMEM supplemented with 15% FBS.

    Techniques: Expressing, Quantitative RT-PCR, Incubation, Control, Staining, Software

    Collagens and fibroblasts inhibit oncolytic virus penetration and reduce antitumor effects (A) T3-2D, MKN45, MEF, and YS-1 cells were infected with OBP-702 at the indicated MOIs for 3 days. Cell viability was assessed using the XTT assays. Cell viability was calculated relative to that of the mock-infected cells, which were set as 1.0. Data are expressed as the mean ± SD ( n = 5). (B) T3-2D and MKN45 cells were infected with OBP-702 at the indicated MOIs for 3 days with or without 10% collagen containing medium. Cell viability was assessed using the XTT assays. Cell viability was calculated relative to that of the mock-infected cells, which were set as 1.0. Data are expressed as the mean ± SD ( n = 5). (C) Representative cellular morphological images of T3-2D and MKN45 cells infected with 100 MOI of OBP-702 with or without 10% collagen stimulation for 72 h. Scale bars, 100 μm. (D) Representative spheroid morphological images of T3-2D cells infected with 20 MOI of OBP-702 or MKN45 cells infected with 50 MOI of OBP-702 with or without 2% collagen stimulation for 7 days. Scale bars, 100 μm. (E) ATP cell viability assay of T3-2D and MKN45 spheroids with or without 2% collagen stimulation for 7 days after infection with OBP-702 (20 MOI or 50 MOI). Data are expressed as the mean ± SD ( n = 5). (F) Representative images of mono-spheroids and co-cultured spheroids infected with OBP-401 (100 MOI) for 48 h. T3-2D and MKN45 cells were labeled with red cell trackers and MEF and YS-1 cells with blue cell trackers. Scale bars, 50 μm. ∗∗ p < 0.01, ∗∗∗ p < 0.001.

    Journal: Molecular Therapy Oncology

    Article Title: Collagen depletion by pirfenidone enhances antitumor effect of oncolytic adenovirus against peritoneal metastases of gastric cancer

    doi: 10.1016/j.omton.2025.201045

    Figure Lengend Snippet: Collagens and fibroblasts inhibit oncolytic virus penetration and reduce antitumor effects (A) T3-2D, MKN45, MEF, and YS-1 cells were infected with OBP-702 at the indicated MOIs for 3 days. Cell viability was assessed using the XTT assays. Cell viability was calculated relative to that of the mock-infected cells, which were set as 1.0. Data are expressed as the mean ± SD ( n = 5). (B) T3-2D and MKN45 cells were infected with OBP-702 at the indicated MOIs for 3 days with or without 10% collagen containing medium. Cell viability was assessed using the XTT assays. Cell viability was calculated relative to that of the mock-infected cells, which were set as 1.0. Data are expressed as the mean ± SD ( n = 5). (C) Representative cellular morphological images of T3-2D and MKN45 cells infected with 100 MOI of OBP-702 with or without 10% collagen stimulation for 72 h. Scale bars, 100 μm. (D) Representative spheroid morphological images of T3-2D cells infected with 20 MOI of OBP-702 or MKN45 cells infected with 50 MOI of OBP-702 with or without 2% collagen stimulation for 7 days. Scale bars, 100 μm. (E) ATP cell viability assay of T3-2D and MKN45 spheroids with or without 2% collagen stimulation for 7 days after infection with OBP-702 (20 MOI or 50 MOI). Data are expressed as the mean ± SD ( n = 5). (F) Representative images of mono-spheroids and co-cultured spheroids infected with OBP-401 (100 MOI) for 48 h. T3-2D and MKN45 cells were labeled with red cell trackers and MEF and YS-1 cells with blue cell trackers. Scale bars, 50 μm. ∗∗ p < 0.01, ∗∗∗ p < 0.001.

    Article Snippet: A murine embryonic fibroblast (MEF) cell line was purchased from the American Type Culture Collection (Manassas, VA) and maintained in DMEM supplemented with 15% FBS.

    Techniques: Virus, Infection, Viability Assay, Cell Culture, Labeling