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Isolation of Mouse Lung Dendritic Cells
Published on: November 22, 2011
CD208/dendritic cell-lysosomal associated membrane protein is a marker of normal and transformed type II pneumocytes
Bruno Salaun1, Blandine de Saint-Vis, Nathalie Pacheco
1Laboratory for Immunological Research, Schering Plough Research Institute, Dardilly, France.
Insights
Dendritic cell-lysosomal associated membrane protein (DC-LAMP) is constitutively expressed in normal lung pneumocytes. This protein also marks transformed type II pneumocytes, aiding lung adenocarcinoma classification.
Area of Science:
- Immunology
- Cell Biology
- Pulmonology
Background:
- Dendritic cell-lysosomal associated membrane protein (DC-LAMP) is a lysosomal associated membrane protein (LAMP) family member.
- DC-LAMP is expressed by human dendritic cells (DCs) upon activation, but its mouse counterpart is not detected in mature DCs.
Purpose of the Study:
- To investigate the expression and localization of DC-LAMP in normal and transformed lung cells.
- To determine if DC-LAMP serves as a potential biomarker for lung adenocarcinomas.
Main Methods:
- Confocal microscopy
- Immunoelectron microscopy
- Analysis of human, mouse, and sheep lung tissues
- Analysis of bronchioloalveolar carcinoma and ovine pulmonary adenocarcinoma samples
Main Results:
- DC-LAMP is constitutively expressed in mouse, sheep, and human type II pneumocytes.
- In mouse type II pneumocytes, DC-LAMP co-localizes with lamellar body markers and intracellular MHC class II molecules.
- DC-LAMP is expressed in human bronchioloalveolar carcinoma cells and ovine pulmonary adenocarcinoma, a model for human lung adenocarcinoma.
Conclusions:
- DC-LAMP is constitutively expressed in normal type II pneumocytes.
- DC-LAMP serves as a marker for transformed type II pneumocytes.
- DC-LAMP may aid in the study and classification of human lung adenocarcinomas.
Abstract:
Dendritic cell-lysosomal associated membrane protein (DC-LAMP)/CD208, a member of the lysosomal associated membrane protein (LAMP) family, is specifically expressed by human DCs on activation. However, its mouse counterpart could not be detected in mature DCs. The present study demonstrates that DC-LAMP is constitutively expressed by mouse, sheep, and human type II pneumocytes. Confocal and immunoelectron microscopy showed that mouse DC-LAMP protein co-localizes with lbm180, a specific marker for the limiting membrane of lamellar bodies that contain surfactant protein B, as well as with intracellular MHC class II molecules that accumulate in the same organelles. Expression of DC-LAMP was also occasionally detected at the cell surface of type II pneumocytes. Interestingly, human bronchioloalveolar carcinoma tumor cells, which correspond to transformed type II pneumocytes, express DC-LAMP. Similar observations were made in the Jaagsiekte sheep retrovirus-associated ovine pulmonary adenocarcinoma, a model of human bronchioloalveolar carcinoma. This study establishes that DC-LAMP is constitutively expressed in normal type II pneumocytes. Furthermore, DC-LAMP appears to be a marker of transformed type II pneumocytes as well, an observation that may help the study and the classification of human lung adenocarcinomas.

