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Expression patterns of protein C inhibitor in mouse development
Authors:Gerry T. M. Wagenaar  Pavel Uhrin  Klara Weipoltshammer  Marlene Almeder  Pieter S. Hiemstra  Margarethe Geiger  Joost C. M. Meijers  Christian Schöfer
Affiliation:(1) Department of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands;(2) Department of Clinical Chemistry and Haematology, University Medical Center, Utrecht, The Netherlands;(3) Department of Vascular Biology and Thrombosis Research, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria;(4) Department for Cell- and Developmental Biology, Developmental Biology and Functional Microscopy, Center for Anatomy and Cell Biology, Medical University of Vienna, Vienna, Austria;(5) Department of Pulmonology, Leiden University Medical Center, Leiden, The Netherlands;(6) Departments of Vascular Medicine and Experimental Vascular Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands;
Abstract:Proteolysis of extracellular matrix is an important requirement for embryonic development and is instrumental in processes such as morphogenesis, angiogenesis, and cell migration. Efficient remodeling requires controlled spatio-temporal expression of both the proteases and their inhibitors. Protein C inhibitor (PCI) effectively blocks a range of serine proteases, and recently has been suggested to play a role in cell differentiation and angiogenesis. In this study, we mapped the expression pattern of PCI throughout mouse development using in situ hybridization and immunohistochemistry. We detected a wide-spread, yet distinct expression pattern with prominent PCI levels in skin including vibrissae, and in fore- and hindgut. Further sites of PCI expression were choroid plexus of brain ventricles, heart, skeletal muscles, urogenital tract, and cartilages. A strong and stage-dependent PCI expression was observed in the developing lung. In the pseudoglandular stage, PCI expression was present in distal branching tubules whereas proximal tubules did not express PCI. Later in development, in the saccular stage, PCI expression was restricted to distal bronchioli whereas sacculi did not express PCI. PCI expression declined in postnatal stages and was not detected in adult lungs. In general, embryonic PCI expression indicates multifunctional roles of PCI during mouse development. The expression pattern of PCI during lung development suggests its possible involvement in lung morphogenesis and angiogenesis.
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