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2 results on '"Nadine Hartjen"'

1. Evaluation of surfactant proteins A, B, C, and D in articular cartilage, synovial membrane and synovial fluid of healthy as well as patients with osteoarthritis and rheumatoid arthritis.

Author

Nadine Hartjen, Lars Bräuer, Beate Reiß, Horst Claassen, Stephanie Beileke, Fabian Garreis, Sebastian Hoogeboom, Michael Tsokos, Saskia Etzold, Brigitte Müller-Hilke, Kolja Gelse, Thomas Müller, Mary B Goldring, Friedrich Paulsen, and Martin Schicht

Subjects
Medicine, Science
Abstract

OBJECTIVE:Surfactant Proteins (SPs) are well known from lung and form, along with phospholipids, a surface-active-layer at the liquid-air-interface of the alveolar lining. They play a major protective role by lowering surface tension, activating innate and adaptive immune defense at the lung mucosal interface, especially during infection. We analyzed the regulation of SPs in human and mouse articular chondrocytes, synoviocytes, and synovial fluid under healthy and inflammatory conditions, as well as in tissues of patients suffering from osteoarthritis and rheumatoid arthritis. METHODS:Immunohistochemistry, RT-PCR, qRT-PCR, ELISA, Western blotting were performed in cell cultures and tissue samples to determine localization, regulation, and concentration of SPs. RESULTS:All four SPs, were expressed by healthy human and mouse articular chondrocytes and synoviocytes and were also present in synovial fluid. Treatment with inflammatory mediators like IL-1β and TNF-α led to short-term upregulation of individual SPs in vitro. In tissues from patients with osteoarthritis and rheumatoid arthritis, protein levels of all four SPs increased significantly compared to the controls used. CONCLUSION:These results show the distribution and amount of SPs in tissues of articular joints. They are produced by chondrocytes and synoviocytes and occur in measurable amounts in synovial fluid. All four SPs seem to be differently regulated under pathologic conditions. Their physiological functions in lowering surface tension and immune defense need further elucidation and make them potential candidates for therapeutic intervention.

Published
2018
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2. Palate Lung Nasal Clone (PLUNC), a Novel Protein of the Tear Film: Three-Dimensional Structure, Immune Activation, and Involvement in Dry Eye Disease (DED)

Author

Friedrich E. Kruse, C. Jacobi, Felix Rausch, Fabian Garreis, Friedrich Paulsen, Martin Beron, Stephanie Beileke, Nadine Hartjen, Lars Bräuer, and Martin Schicht

Subjects
Adult, Male, Pathology, medicine.medical_specialty, Blotting, Western, Clone (cell biology), Dry Eye Syndromes, Enzyme-Linked Immunosorbent Assay, Plunc, Biology, Polymerase Chain Reaction, Cell Line, Proinflammatory cytokine, Imaging, Three-Dimensional, medicine, Humans, Vision, Ocular, Aged, Glycoproteins, chemistry.chemical_classification, Lung, Osmolar Concentration, Middle Aged, Phosphoproteins, Immunohistochemistry, eye diseases, medicine.anatomical_structure, Gene Expression Regulation, chemistry, Tears, RNA, Female, sense organs, Glycoprotein
Abstract

PURPOSE Palate Lung Nasal Clone (PLUNC) is a hydrophobic protein belonging to the family of surfactant proteins that is involved in fluid balance regulation of the lung. Moreover, it is known to directly act against gram-negative bacteria. The purpose of this study was to investigate the possible expression and antimicrobial role of PLUNC at the healthy ocular surface and in tears of patients suffering from dry eye disease (DED). METHODS Bioinformatics and biochemical and immunologic methods were combined to elucidate the structure and function of PLUNC at the ocular surface. Tissue-specific localization was performed by using immunohistochemistry. The PLUNC levels in tear samples from non-Sjogren's DED patients with moderate dry eye suffering either from hyperevaporation or tear deficiency were analyzed by ELISA and compared with tears from healthy volunteers. RESULTS Palate Lung Nasal Clone is expressed under healthy conditions at the ocular surface and secreted into the tear film. Protein modeling studies and molecular dynamics simulations performed indicated surface activity of PLUNC. In vitro experiments revealed that proinflammatory cytokines and bacterial supernatants have only a slight effect on the expression of PLUNC in HCE and HCjE cell lines. In tears from DED patients, the PLUNC concentration is significantly increased (7-fold in evaporative dry eye tears and 17-fold in tears from patients with tear deficiency) compared with healthy subjects. CONCLUSIONS The results show that PLUNC is a protein of the tear film and suggest that it plays a role in fluid balance and surface tension regulation at the ocular surface.

Published
2015
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