Immunohistochemical analysis of MCC, TARC and CD 104 antigens in human lung tissue.

Objective: The aim of this study was to investigate the the distribution of CMA1 protein (MCC), CCL17 protein (TARC) and Integrin beta 4 (CD 104) monoclonal antibodies in normal adult human lung tissue. Material and Methods: In this study we examined the lung biopsy specimens obtained from the adult...

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Publicado en:Turkiye Klinikleri Journal of Medical Sciences Vol. 30; no. 6; pp. 1971 - 1979
Autores principales: Korkmaz, Metin, Akkus, Murat, Yildirim, Ayse, Baran, Özlem Pamukcu, Aktas, Ayfer
Formato: research tables/charts Journal Article
Publicado: Turkiye Klinikleri Dec2010
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Dec2010
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      pub: Turkiye Klinikleri
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        104812800
        2010937945
        10.5336/medsci.2009-13920
        104812800
      ppf: 1971
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        atl: Immunohistochemical analysis of MCC, TARC and CD 104 antigens in human lung tissue.
      aug:
        au:
          Korkmaz, Metin
          Akkus, Murat
          Yildirim, Ayse
          Baran, Özlem Pamukcu
          Aktas, Ayfer
        affil: Department of Histology and Embriology, Bursa State Hospital, Bursa
      sug:
        subj:
          Antigens
          Immunohistochemistry
          Lung Physiology
          Proteins
          Academic Medical Centers
          Biopsy
          Human
          In Vitro Studies
          Turkiye
      ab: Objective: The aim of this study was to investigate the the distribution of CMA1 protein (MCC), CCL17 protein (TARC) and Integrin beta 4 (CD 104) monoclonal antibodies in normal adult human lung tissue. Material and Methods: In this study we examined the lung biopsy specimens obtained from the adult patients who underwent operations for different reasons in the Department of Lung Surgery at Dicle University Hospital, Diyarbak?r, Turkey. The tissue samples were immediately frozen in liquid nitrogen at -196º C. The samples were immunostained by indirect immune peroxidase technique. As primary antibodies, MCC, TARC and CD104 were used. As secondary antibodies, 1:200 rabbit anti - mouse IgG peroxidase diluted in PBS/BSA and 1:100 normal human serum solution were used. Negative control staining was performed using irrelevant mouse monoclonal antibodies omitting the primary antibody step. Sections were examined and photographed by Olympus BH2 light microscope. Results: We observed moderate reaction with vascular endothelial cells and with vascular smooth muscle cells with MCC which was aimed to show overall the presence of human lung mast cells. TARC, which was aimed to express the follicular dentritic cells, moderately reacted with follicular dentritic cells, bronchial smooth muscle cells and vascular endothelial cells. CD104, which is the integrin ?4 subunit that plays an important role in the adhesion of epithelium to basement membranes, moderately reacted with vascular endothelial cells and mainly reacted with the follicular dentritic cells of bronchi. Conclusion: In our study, it was defined that the expressions of these molecules have important role in understanding the function of human lung tissue. We reached the conclusion that our study, by presenting the difference between the normal lung tissue and pathologic lung tissue with expression the related proteins immunohistochemically may constitute preliminary findings for excluding the diseases like interstisial lung disease or chronic obstructive lung disease for the aim of. Our preliminary findings may shed light on future studies.
      pubtype: Academic Journal
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        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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