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human acp5 elisa kit  (Boster Bio)


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    Boster Bio human acp5 elisa kit
    Inhibition of <t>ACP5</t> suppresses CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels after ACP5 silencing ( n = 3/group). ( B - C ) Western blot analysis of the silencing efficiency of ACP5 ( n = 3/group). ( D - E ) EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 4/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n ≥ 3/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05
    Human Acp5 Elisa Kit, supplied by Boster Bio, 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/human+acp5+elisa+kit/pmc11179352-79-14-21?v=Boster+Bio
    Average 93 stars, based on 1 article reviews
    human acp5 elisa kit - by Bioz Stars, 2026-07
    93/100 stars

    Images

    1) Product Images from "Inhibition of tartrate-resistant acid phosphatase 5 can prevent cardiac fibrosis after myocardial infarction"

    Article Title: Inhibition of tartrate-resistant acid phosphatase 5 can prevent cardiac fibrosis after myocardial infarction

    Journal: Molecular Medicine

    doi: 10.1186/s10020-024-00856-1

    Inhibition of ACP5 suppresses CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels after ACP5 silencing ( n = 3/group). ( B - C ) Western blot analysis of the silencing efficiency of ACP5 ( n = 3/group). ( D - E ) EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 4/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n ≥ 3/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05
    Figure Legend Snippet: Inhibition of ACP5 suppresses CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels after ACP5 silencing ( n = 3/group). ( B - C ) Western blot analysis of the silencing efficiency of ACP5 ( n = 3/group). ( D - E ) EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 4/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n ≥ 3/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Techniques Used: Inhibition, Migration, Expressing, Western Blot, EdU Assay, Wound Healing Assay

    Overexpression of ACP5 promotes CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels of ACP5 and the overexpression efficiency ( n = 4/group). ( B - C ) Western blot analysis of the overexpression efficiency of ACP5 ( n = 3/group). ( D - E ) The EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 3/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n = 4/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05
    Figure Legend Snippet: Overexpression of ACP5 promotes CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels of ACP5 and the overexpression efficiency ( n = 4/group). ( B - C ) Western blot analysis of the overexpression efficiency of ACP5 ( n = 3/group). ( D - E ) The EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 3/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n = 4/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Techniques Used: Over Expression, Migration, Expressing, Western Blot, EdU Assay, Wound Healing Assay

    ACP5 inhibition suppresses fibrosis in MI mice and enhances cardiac function. ( A ) Masson staining and Sirius red staining in each group ( n = 6/group; upper layer, scale bar = 1000 μm; middle layer, scale bar = 100 μm; lower layer, scale bar = 100 μm). ( B ) Masson staining of fibrosis. ( C ) Sirius red staining of the collagen area. ( D ) Representative images of echocardiography. ( E - F ) Echocardiographic measurements of LVEF (E) and LVFS (F) ( n = 6/group). ( G - I ) Western blot analysis of α-SMA and COL1 in the hearts of mice in different groups ( n = 3/group). ( J - K ) Immunofluorescence staining of α-SMA in the hearts of mice in different groups ( n = 4/group); scale bar = 50 μm. (The bottom-layer image in Fig. 4J is the locally enlarged image circled in the Merge graph, bar = 20 μm). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05
    Figure Legend Snippet: ACP5 inhibition suppresses fibrosis in MI mice and enhances cardiac function. ( A ) Masson staining and Sirius red staining in each group ( n = 6/group; upper layer, scale bar = 1000 μm; middle layer, scale bar = 100 μm; lower layer, scale bar = 100 μm). ( B ) Masson staining of fibrosis. ( C ) Sirius red staining of the collagen area. ( D ) Representative images of echocardiography. ( E - F ) Echocardiographic measurements of LVEF (E) and LVFS (F) ( n = 6/group). ( G - I ) Western blot analysis of α-SMA and COL1 in the hearts of mice in different groups ( n = 3/group). ( J - K ) Immunofluorescence staining of α-SMA in the hearts of mice in different groups ( n = 4/group); scale bar = 50 μm. (The bottom-layer image in Fig. 4J is the locally enlarged image circled in the Merge graph, bar = 20 μm). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Techniques Used: Inhibition, Staining, Western Blot, Immunofluorescence

    ACP5 affects the GSK3β/β-catenin signal transduction pathway. ( A - D ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in ACP5-deficient CFs ( n = 3/group). ( E - H ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in CFs overexpressing ACP5 ( n = 3/group). ( I - L ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in the hearts of mice in different groups ( n ≥ 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05
    Figure Legend Snippet: ACP5 affects the GSK3β/β-catenin signal transduction pathway. ( A - D ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in ACP5-deficient CFs ( n = 3/group). ( E - H ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in CFs overexpressing ACP5 ( n = 3/group). ( I - L ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in the hearts of mice in different groups ( n ≥ 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Techniques Used: Transduction, Western Blot, Expressing

    ACP5 affects CF activation by regulating ERK. ( A - B ) Western blot analysis of the expression levels of p-ERK and ERK in ACP5-deficient CFs ( n = 3/group). ( C - D ) Western blot analysis of the expression levels of p-ERK and ERK in CFs overexpressing ACP5 ( n = 3/group). ( E - F ) Western blot analysis of the expression levels of p-ERK and ERK in the hearts of mice in different groups ( n = 3/group). ( G - K ) Western blot analysis of the expression levels of ACP5, p-ERK, ERK, p-GSK3β, GSK3β, and β-catenin in CFs pretreated with Ro 67-7476 (an ERK agonist) ( n = 3/group). ( L - M ) The EdU assay was used to detect the proliferation rate of CFs pretreated with Ro 67-7476 (an ERK agonist) ( n = 4/group); scale bar = 100 μm. ( N - O ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( P - R ) Western blot analysis of α-SMA and COL1 in the hearts of mice in different groups ( n = 3/group).* P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05
    Figure Legend Snippet: ACP5 affects CF activation by regulating ERK. ( A - B ) Western blot analysis of the expression levels of p-ERK and ERK in ACP5-deficient CFs ( n = 3/group). ( C - D ) Western blot analysis of the expression levels of p-ERK and ERK in CFs overexpressing ACP5 ( n = 3/group). ( E - F ) Western blot analysis of the expression levels of p-ERK and ERK in the hearts of mice in different groups ( n = 3/group). ( G - K ) Western blot analysis of the expression levels of ACP5, p-ERK, ERK, p-GSK3β, GSK3β, and β-catenin in CFs pretreated with Ro 67-7476 (an ERK agonist) ( n = 3/group). ( L - M ) The EdU assay was used to detect the proliferation rate of CFs pretreated with Ro 67-7476 (an ERK agonist) ( n = 4/group); scale bar = 100 μm. ( N - O ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( P - R ) Western blot analysis of α-SMA and COL1 in the hearts of mice in different groups ( n = 3/group).* P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Techniques Used: Activation Assay, Western Blot, Expressing, EdU Assay, Migration

    Schematic diagram of the mechanism of ACP5 in myocardial fibrosis after MI. Under the stimulation of MI or Ang II, the increased expression of ACP5 activates the ERK/GSK3β/β-catenin signaling pathway, which promotes the transformation of CFs into myofibroblasts with more active proliferation, migration and fibrosis, leading to the onset of myocardial fibrosis. (Generated by Figdraw)
    Figure Legend Snippet: Schematic diagram of the mechanism of ACP5 in myocardial fibrosis after MI. Under the stimulation of MI or Ang II, the increased expression of ACP5 activates the ERK/GSK3β/β-catenin signaling pathway, which promotes the transformation of CFs into myofibroblasts with more active proliferation, migration and fibrosis, leading to the onset of myocardial fibrosis. (Generated by Figdraw)

    Techniques Used: Expressing, Transformation Assay, Migration, Generated



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    Inhibition of <t>ACP5</t> suppresses CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels after ACP5 silencing ( n = 3/group). ( B - C ) Western blot analysis of the silencing efficiency of ACP5 ( n = 3/group). ( D - E ) EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 4/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n ≥ 3/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05
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    Inhibition of <t>ACP5</t> suppresses CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels after ACP5 silencing ( n = 3/group). ( B - C ) Western blot analysis of the silencing efficiency of ACP5 ( n = 3/group). ( D - E ) EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 4/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n ≥ 3/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05
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    Image Search Results


    Inhibition of ACP5 suppresses CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels after ACP5 silencing ( n = 3/group). ( B - C ) Western blot analysis of the silencing efficiency of ACP5 ( n = 3/group). ( D - E ) EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 4/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n ≥ 3/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Journal: Molecular Medicine

    Article Title: Inhibition of tartrate-resistant acid phosphatase 5 can prevent cardiac fibrosis after myocardial infarction

    doi: 10.1186/s10020-024-00856-1

    Figure Lengend Snippet: Inhibition of ACP5 suppresses CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels after ACP5 silencing ( n = 3/group). ( B - C ) Western blot analysis of the silencing efficiency of ACP5 ( n = 3/group). ( D - E ) EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 4/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n ≥ 3/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Article Snippet: The Mouse ACP5 ELISA Kit was purchased from Signalway Antibody (USA, #EK12408), and the Human ACP5 ELISA Kit was purchased from BOSTER (China, #EK2138).

    Techniques: Inhibition, Migration, Expressing, Western Blot, EdU Assay, Wound Healing Assay

    Overexpression of ACP5 promotes CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels of ACP5 and the overexpression efficiency ( n = 4/group). ( B - C ) Western blot analysis of the overexpression efficiency of ACP5 ( n = 3/group). ( D - E ) The EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 3/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n = 4/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Journal: Molecular Medicine

    Article Title: Inhibition of tartrate-resistant acid phosphatase 5 can prevent cardiac fibrosis after myocardial infarction

    doi: 10.1186/s10020-024-00856-1

    Figure Lengend Snippet: Overexpression of ACP5 promotes CF proliferation, migration, and transition into myofibroblasts. ( A ) Relative mRNA expression levels of ACP5 and the overexpression efficiency ( n = 4/group). ( B - C ) Western blot analysis of the overexpression efficiency of ACP5 ( n = 3/group). ( D - E ) The EdU assay was used to detect the cell proliferation rate of CFs ( n = 4/group); scale bar = 100 μm. ( F ) OD values of CFs in different groups ( n = 3/group). ( G - H ) Cell migration was assessed by a wound-healing assay ( n = 4/group); scale bar = 100 μm. ( I - J ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( K - N ) Relative mRNA expression levels of ACP5, α-SMA, COL1, and COL3 in CFs in different groups ( n = 4/group). ( O - Q ) Western blot analysis of α-SMA and COL1 ( n = 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Article Snippet: The Mouse ACP5 ELISA Kit was purchased from Signalway Antibody (USA, #EK12408), and the Human ACP5 ELISA Kit was purchased from BOSTER (China, #EK2138).

    Techniques: Over Expression, Migration, Expressing, Western Blot, EdU Assay, Wound Healing Assay

    ACP5 inhibition suppresses fibrosis in MI mice and enhances cardiac function. ( A ) Masson staining and Sirius red staining in each group ( n = 6/group; upper layer, scale bar = 1000 μm; middle layer, scale bar = 100 μm; lower layer, scale bar = 100 μm). ( B ) Masson staining of fibrosis. ( C ) Sirius red staining of the collagen area. ( D ) Representative images of echocardiography. ( E - F ) Echocardiographic measurements of LVEF (E) and LVFS (F) ( n = 6/group). ( G - I ) Western blot analysis of α-SMA and COL1 in the hearts of mice in different groups ( n = 3/group). ( J - K ) Immunofluorescence staining of α-SMA in the hearts of mice in different groups ( n = 4/group); scale bar = 50 μm. (The bottom-layer image in Fig. 4J is the locally enlarged image circled in the Merge graph, bar = 20 μm). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Journal: Molecular Medicine

    Article Title: Inhibition of tartrate-resistant acid phosphatase 5 can prevent cardiac fibrosis after myocardial infarction

    doi: 10.1186/s10020-024-00856-1

    Figure Lengend Snippet: ACP5 inhibition suppresses fibrosis in MI mice and enhances cardiac function. ( A ) Masson staining and Sirius red staining in each group ( n = 6/group; upper layer, scale bar = 1000 μm; middle layer, scale bar = 100 μm; lower layer, scale bar = 100 μm). ( B ) Masson staining of fibrosis. ( C ) Sirius red staining of the collagen area. ( D ) Representative images of echocardiography. ( E - F ) Echocardiographic measurements of LVEF (E) and LVFS (F) ( n = 6/group). ( G - I ) Western blot analysis of α-SMA and COL1 in the hearts of mice in different groups ( n = 3/group). ( J - K ) Immunofluorescence staining of α-SMA in the hearts of mice in different groups ( n = 4/group); scale bar = 50 μm. (The bottom-layer image in Fig. 4J is the locally enlarged image circled in the Merge graph, bar = 20 μm). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Article Snippet: The Mouse ACP5 ELISA Kit was purchased from Signalway Antibody (USA, #EK12408), and the Human ACP5 ELISA Kit was purchased from BOSTER (China, #EK2138).

    Techniques: Inhibition, Staining, Western Blot, Immunofluorescence

    ACP5 affects the GSK3β/β-catenin signal transduction pathway. ( A - D ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in ACP5-deficient CFs ( n = 3/group). ( E - H ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in CFs overexpressing ACP5 ( n = 3/group). ( I - L ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in the hearts of mice in different groups ( n ≥ 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Journal: Molecular Medicine

    Article Title: Inhibition of tartrate-resistant acid phosphatase 5 can prevent cardiac fibrosis after myocardial infarction

    doi: 10.1186/s10020-024-00856-1

    Figure Lengend Snippet: ACP5 affects the GSK3β/β-catenin signal transduction pathway. ( A - D ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in ACP5-deficient CFs ( n = 3/group). ( E - H ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in CFs overexpressing ACP5 ( n = 3/group). ( I - L ) Western blot analysis of the expression levels of ACP5, p-GSK3β, GSK3β, and β-catenin in the hearts of mice in different groups ( n ≥ 3/group). * P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Article Snippet: The Mouse ACP5 ELISA Kit was purchased from Signalway Antibody (USA, #EK12408), and the Human ACP5 ELISA Kit was purchased from BOSTER (China, #EK2138).

    Techniques: Transduction, Western Blot, Expressing

    ACP5 affects CF activation by regulating ERK. ( A - B ) Western blot analysis of the expression levels of p-ERK and ERK in ACP5-deficient CFs ( n = 3/group). ( C - D ) Western blot analysis of the expression levels of p-ERK and ERK in CFs overexpressing ACP5 ( n = 3/group). ( E - F ) Western blot analysis of the expression levels of p-ERK and ERK in the hearts of mice in different groups ( n = 3/group). ( G - K ) Western blot analysis of the expression levels of ACP5, p-ERK, ERK, p-GSK3β, GSK3β, and β-catenin in CFs pretreated with Ro 67-7476 (an ERK agonist) ( n = 3/group). ( L - M ) The EdU assay was used to detect the proliferation rate of CFs pretreated with Ro 67-7476 (an ERK agonist) ( n = 4/group); scale bar = 100 μm. ( N - O ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( P - R ) Western blot analysis of α-SMA and COL1 in the hearts of mice in different groups ( n = 3/group).* P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Journal: Molecular Medicine

    Article Title: Inhibition of tartrate-resistant acid phosphatase 5 can prevent cardiac fibrosis after myocardial infarction

    doi: 10.1186/s10020-024-00856-1

    Figure Lengend Snippet: ACP5 affects CF activation by regulating ERK. ( A - B ) Western blot analysis of the expression levels of p-ERK and ERK in ACP5-deficient CFs ( n = 3/group). ( C - D ) Western blot analysis of the expression levels of p-ERK and ERK in CFs overexpressing ACP5 ( n = 3/group). ( E - F ) Western blot analysis of the expression levels of p-ERK and ERK in the hearts of mice in different groups ( n = 3/group). ( G - K ) Western blot analysis of the expression levels of ACP5, p-ERK, ERK, p-GSK3β, GSK3β, and β-catenin in CFs pretreated with Ro 67-7476 (an ERK agonist) ( n = 3/group). ( L - M ) The EdU assay was used to detect the proliferation rate of CFs pretreated with Ro 67-7476 (an ERK agonist) ( n = 4/group); scale bar = 100 μm. ( N - O ) Cell migration was assessed by Transwell assays ( n = 4/group); scale bar = 100 μm. ( P - R ) Western blot analysis of α-SMA and COL1 in the hearts of mice in different groups ( n = 3/group).* P < 0.05, ** P < 0.01, *** P < 0.001, and ns: P > 0.05

    Article Snippet: The Mouse ACP5 ELISA Kit was purchased from Signalway Antibody (USA, #EK12408), and the Human ACP5 ELISA Kit was purchased from BOSTER (China, #EK2138).

    Techniques: Activation Assay, Western Blot, Expressing, EdU Assay, Migration

    Schematic diagram of the mechanism of ACP5 in myocardial fibrosis after MI. Under the stimulation of MI or Ang II, the increased expression of ACP5 activates the ERK/GSK3β/β-catenin signaling pathway, which promotes the transformation of CFs into myofibroblasts with more active proliferation, migration and fibrosis, leading to the onset of myocardial fibrosis. (Generated by Figdraw)

    Journal: Molecular Medicine

    Article Title: Inhibition of tartrate-resistant acid phosphatase 5 can prevent cardiac fibrosis after myocardial infarction

    doi: 10.1186/s10020-024-00856-1

    Figure Lengend Snippet: Schematic diagram of the mechanism of ACP5 in myocardial fibrosis after MI. Under the stimulation of MI or Ang II, the increased expression of ACP5 activates the ERK/GSK3β/β-catenin signaling pathway, which promotes the transformation of CFs into myofibroblasts with more active proliferation, migration and fibrosis, leading to the onset of myocardial fibrosis. (Generated by Figdraw)

    Article Snippet: The Mouse ACP5 ELISA Kit was purchased from Signalway Antibody (USA, #EK12408), and the Human ACP5 ELISA Kit was purchased from BOSTER (China, #EK2138).

    Techniques: Expressing, Transformation Assay, Migration, Generated