Phenotypic alterations in type II alveolar epithelial cells in CD4T cell mediated lung inflammation-0

Copyright information:Taken from "Phenotypic alterations in type II alveolar epithelial cells in CD4T cell mediated lung inflammation"http://respiratory-research.com/content/8/1/47Respiratory Research 2007;8(1):47-47.Published online 4 Jul 2007PMCID:PMC1939847. transfer of HA-specific CD4T...

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Hauptverfasser: Gereke, Marcus, Gröbe, Lothar, Prettin, Silvia, Kasper, Michael, Deppenmeier, Stefanie, Gruber, Achim D, Enelow, Richard I, Buer, Jan, Bruder, Dunja
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creator Gereke, Marcus
Gröbe, Lothar
Prettin, Silvia
Kasper, Michael
Deppenmeier, Stefanie
Gruber, Achim D
Enelow, Richard I
Buer, Jan
Bruder, Dunja
description Copyright information:Taken from "Phenotypic alterations in type II alveolar epithelial cells in CD4T cell mediated lung inflammation"http://respiratory-research.com/content/8/1/47Respiratory Research 2007;8(1):47-47.Published online 4 Jul 2007PMCID:PMC1939847. transfer of HA-specific CD4T cells (b, b') and SPC-HA/TCR-HA double transgenic mice (c, c'). Lung sections were stained with H&E. Black arrows indicate AEC II, red arrows indicate lymphocytes. No lesions were detectable in the lung of SPC-HA mice. Specifically, type II pneumocytes were completely unchanged (a, a'). A moderate, perivascular and peribronchiolar infiltration with mature lymphocytes was detected in the lung of SPC-HA mice after transfer with HA-specific CD4T cells. Adjacent to these infiltrations, a slight connective tissue edema and a mild infiltration with neutrophils were observed. Type II pneumocytes in the vicinity of the lymphocytic infiltrations were moderately hypertrophic. A few alveolar macrophages were present in the alveoli (b, b'). Moderate, multifocal, perivascular and peribronchiolar infiltrations with lymphocytes were present in the lung of SPC-HA/TCR-HA double transgenic mice. Type II pneumocytes close to the lymphocytic infiltrations were mildly activated and hypertrophic (c, c'). Histological results were corroborated morphometrically by measuring AEC II surface and perimeter to quantify the degree of cellular hypertrophy (n = 15, 3 mice with 5 AEC II per mouse; ± standard deviation). AEC II surface: SPC-HA vs SPC-HA Transfer: P < 0,001), SPC-HA vs SPC-HA/TCR-HA (P < 0,0001), SPC-HA transfer vs SPC-HA/TCR-HA (P < 0,0001). AEC II perimeter: SPC-HA vs SPC-HA Transfer: P < 0,001), SPC-HA vs SPC-HA/TCR-HA (P < 0,001), SPC-HA transfer vs SPC-HA/TCR-HA (P < 0,001). All Student's t-test.
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Lung sections were stained with H&E. Black arrows indicate AEC II, red arrows indicate lymphocytes. No lesions were detectable in the lung of SPC-HA mice. Specifically, type II pneumocytes were completely unchanged (a, a'). A moderate, perivascular and peribronchiolar infiltration with mature lymphocytes was detected in the lung of SPC-HA mice after transfer with HA-specific CD4T cells. Adjacent to these infiltrations, a slight connective tissue edema and a mild infiltration with neutrophils were observed. Type II pneumocytes in the vicinity of the lymphocytic infiltrations were moderately hypertrophic. A few alveolar macrophages were present in the alveoli (b, b'). Moderate, multifocal, perivascular and peribronchiolar infiltrations with lymphocytes were present in the lung of SPC-HA/TCR-HA double transgenic mice. Type II pneumocytes close to the lymphocytic infiltrations were mildly activated and hypertrophic (c, c'). Histological results were corroborated morphometrically by measuring AEC II surface and perimeter to quantify the degree of cellular hypertrophy (n = 15, 3 mice with 5 AEC II per mouse; ± standard deviation). AEC II surface: SPC-HA vs SPC-HA Transfer: P < 0,001), SPC-HA vs SPC-HA/TCR-HA (P < 0,0001), SPC-HA transfer vs SPC-HA/TCR-HA (P < 0,0001). AEC II perimeter: SPC-HA vs SPC-HA Transfer: P < 0,001), SPC-HA vs SPC-HA/TCR-HA (P < 0,001), SPC-HA transfer vs SPC-HA/TCR-HA (P < 0,001). 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Lung sections were stained with H&E. Black arrows indicate AEC II, red arrows indicate lymphocytes. No lesions were detectable in the lung of SPC-HA mice. Specifically, type II pneumocytes were completely unchanged (a, a'). A moderate, perivascular and peribronchiolar infiltration with mature lymphocytes was detected in the lung of SPC-HA mice after transfer with HA-specific CD4T cells. Adjacent to these infiltrations, a slight connective tissue edema and a mild infiltration with neutrophils were observed. Type II pneumocytes in the vicinity of the lymphocytic infiltrations were moderately hypertrophic. A few alveolar macrophages were present in the alveoli (b, b'). Moderate, multifocal, perivascular and peribronchiolar infiltrations with lymphocytes were present in the lung of SPC-HA/TCR-HA double transgenic mice. Type II pneumocytes close to the lymphocytic infiltrations were mildly activated and hypertrophic (c, c'). Histological results were corroborated morphometrically by measuring AEC II surface and perimeter to quantify the degree of cellular hypertrophy (n = 15, 3 mice with 5 AEC II per mouse; ± standard deviation). AEC II surface: SPC-HA vs SPC-HA Transfer: P < 0,001), SPC-HA vs SPC-HA/TCR-HA (P < 0,0001), SPC-HA transfer vs SPC-HA/TCR-HA (P < 0,0001). AEC II perimeter: SPC-HA vs SPC-HA Transfer: P < 0,001), SPC-HA vs SPC-HA/TCR-HA (P < 0,001), SPC-HA transfer vs SPC-HA/TCR-HA (P < 0,001). 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Lung sections were stained with H&E. Black arrows indicate AEC II, red arrows indicate lymphocytes. No lesions were detectable in the lung of SPC-HA mice. Specifically, type II pneumocytes were completely unchanged (a, a'). A moderate, perivascular and peribronchiolar infiltration with mature lymphocytes was detected in the lung of SPC-HA mice after transfer with HA-specific CD4T cells. Adjacent to these infiltrations, a slight connective tissue edema and a mild infiltration with neutrophils were observed. Type II pneumocytes in the vicinity of the lymphocytic infiltrations were moderately hypertrophic. A few alveolar macrophages were present in the alveoli (b, b'). Moderate, multifocal, perivascular and peribronchiolar infiltrations with lymphocytes were present in the lung of SPC-HA/TCR-HA double transgenic mice. Type II pneumocytes close to the lymphocytic infiltrations were mildly activated and hypertrophic (c, c'). Histological results were corroborated morphometrically by measuring AEC II surface and perimeter to quantify the degree of cellular hypertrophy (n = 15, 3 mice with 5 AEC II per mouse; ± standard deviation). AEC II surface: SPC-HA vs SPC-HA Transfer: P < 0,001), SPC-HA vs SPC-HA/TCR-HA (P < 0,0001), SPC-HA transfer vs SPC-HA/TCR-HA (P < 0,0001). AEC II perimeter: SPC-HA vs SPC-HA Transfer: P < 0,001), SPC-HA vs SPC-HA/TCR-HA (P < 0,001), SPC-HA transfer vs SPC-HA/TCR-HA (P < 0,001). All Student's t-test.]]></abstract><pub>figshare</pub><doi>10.6084/m9.figshare.60306</doi><oa>free_for_read</oa></addata></record>
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title Phenotypic alterations in type II alveolar epithelial cells in CD4T cell mediated lung inflammation-0
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