8 research outputs found

    LITAF protein levels are increased in LPM harvested from inflamed colonic tissue and further increased in inflamed LPM following LPS (1 ug/mL) stimulation (N = 5).

    No full text
    <p><b><i>A</i></b>) Western blot of LITAF levels and GAPDH levels in freshly harvested LPM from Non-Inflamed and Inflamed colonic tissue. The graph shows the optical density (OD) of LITAF levels normalized to GAPDH levels. * Statistical difference from Non-Inflamed group (p<0.05). B) Western blot of LITAF levels and β-Actin levels in LPM harvested from inflamed colonic tissue stimulated with LPS ex vivo compared to LPM harvested from inflamed colonic tissue, but not treated with LPS (Non-treated). The graph show OD of LITAF levels normalized to β-Actin levels. * Statistical difference (p<0.05).</p

    TNBS-induced inflammation in C57BL/6 Mice.

    No full text
    <p>Inflammation was induced by TNBS (1.5 mg, in 50% ethanol solution) and animals were monitored for: A) Colonic tissue was collected and assessed for MPO activity (N = 4, except Day 1, N = 3). Data are expressed as % Day 0 Control ± SEM. <sup>#</sup> Statistical difference (p<0.001). <b><i>B</i></b>) Representative histological images of colonic tissue from C57BL/6 mice 24 hours following TNBS administration showing colonic inflammation (Mag 100×).</p

    TNBS-induced histological damage is not reduced in LITAF mac -/- mice.

    No full text
    <p><b><i>A</i></b>) Representative histological images of colonic inflammation: Untreated Control; TNBS 24 hours; and, TNBS 48 hours following TNBS administration. (N = 3) images (Mag 100×). <b><i>B</i></b>) Histological score (0–4) ± SEM (N = 5) of colonic tissue 24 and 48 hours following TNBS administration.</p

    LPM harvested from LITAF macrophage specific knockout mice (LITAF mac -/- mice) produce less TNF-α than LPM harvested from C57BL/6 mice.

    No full text
    <p><b><i>A</i></b>) Western blot of LITAF and Actin confirming the knockout of LITAF protein in peritoneal macrophages harvested from LITAF mac -/- and C57BL/6 mice. <b><i>B</i></b>) TNF-α secretion from inflamed LPM isolated from colonic tissues of LITAF mac -/- (N = 6) or wildtype C57BL/6 (N = 12) following LPS stimulation (24 hours). Data are expressed as % Inflamed C57BL/6 group ± SEM. * Statistical difference (p<0.05), # statistical difference (p<0.001).</p

    TNF-α message levels from inflamed colonic tissue harvested from LITAF macrophage specific mice (LITAF mac -/- mice) is reduced compared to C57BL/6 mice.

    No full text
    <p>TNF-α message levels were measured in colonic tissue following TNBS administration (0.3 mg) for 24 hrs in LITAF mac -/- mice (N = 6) and C57BL/6 mice (N = 12). Data are expressed as % Non-Inflamed control ± SEM. * Statistical difference (p<0.05).</p

    LITAF macrophage specific knockout mice (LITAF mac -/-) show reduced changes in bodyweight and MPO following TNBS administration.

    No full text
    <p><b><i>A</i></b>) Following TNBS (3.0 mg) administration to LITAF mac -/- mice (N = 6) and C57BL/6 mice (N = 6), bodyweights were measured 24 hours later. Data are expressed as % initial (day 0) bodyweight. * Statistical difference (p<0.05), # statistical difference (p<0.001). B) Following TNBS (3.0 mg) administration to LITAF mac -/- mice (N = 6) and C57BL/6 mice (N = 6), colonic tissue was collected and assessed for MPO activity. Data are expressed as % Non-inflamed MPO activity. <sup>#</sup> Statistical difference (p<0.001).</p

    Secreted TNF-α levels from LPM harvested from inflamed colonic tissue are reduced with the administration of signaling inhibitors.

    No full text
    <p><b><i>A</i></b>) Secreted TNF-α from LPM harvested from inflamed colonic tissue are reduced when administered p38 inhibitor (SB-202190) prior to, and throughout LPS (1 ug/mL) stimulation (24 hours) (N = 8). Data are expressed as % Inflamed DMSO vehicle ±SEM. * Statistical difference (p<0.05), <sup>#</sup> statistical difference (p<0.001). B) Secreted TNF-α from LPM harvested from inflamed colonic tissue are reduced when administered NF-κB inhibitor (BAY 11-7082) prior to, and throughout LPS (1 ug/mL) stimulation (24 hours) (N = 6). Data are expressed as % Inflamed DMSO Vehicle group ± SEM. <sup>#</sup> Statistical difference (p<0.001).</p

    Secreted TNF-α levels and LITAF message are increased in LPM harvested from inflamed colonic tissue compared to LPM harvested from non-inflamed colonic tissue.

    No full text
    <p><b><i>A</i></b>) Following TNBS administration, LPM were harvested and stimulated with LPS (1 ug/mL) <i>ex vivo</i> (24 hours) and TNF-α secretion was measured (N = 8). Data are presented as % Non-Inflamed Non-treated control ± SEM. * Statistical difference (p<0.05), # statistical difference (p<0.001). B) LITAF message levels are increased in LPM harvested from inflamed colonic tissue following LPS (1 ug/mL) stimulation (1 hour) compared to LPM harvested from non-inflamed colonic tissue (N = 7 for Non-treated, N = 8 LPS treated). Data were normalized to β-Actin message and presented as % Non-Inflamed Non-treated group ± SEM. * Statistical difference (p<0.05).</p
    corecore