Background: Lung macrophages, that is, the intravascular, interstitial, pleural, and surface macrophages, are part of the mononuclear phagocyte system. They are derived from the hematopoietic stem cell in the bone marrow with the monocytes as their putative precursors. Macrophages residing on the inner surfaces of the lungs and immersed within the lung lining layer, that is, the alveolar and the airway macrophages, are constantly exposed to the environment; it is those cells that are recognized as first line of cellular host defense. Methods and Results: Phagocytic uptake of inhaled and deposited particles is the main mechanism to remove insoluble micrometer-sized particles from the lung surfaces, where mucociliary transport, cough, or sneezing fail or are absent. Phagocytosis requires an intact cytoskeleton and is most efficient when mediated by Fc-receptors, but complement and scavenger receptors like MARCO and CD206 are just as important. The main pathway for the clearance of macrophage-associ...

Update on Macrophage Clearance of Inhaled Micro- and Nanoparticles

Activated PMN Exosomes: Pathogenic Entities Causing Matrix Destruction and Disease in the Lung.

The pulmonary vasculature comprises three anatomic compartments connected in series: the arterial tree, an extensive capillary bed, and the venular tree. Although, in general, this vasculature is thin-walled, structure is nonetheless complex. Contributions to structure (and thus potentially to function) from cells other than endothelial and smooth muscle cells as well as those from the extracellular matrix should be considered. This review is multifaceted, bringing together information regarding (i) classification of pulmonary vessels, (ii) branching geometry in the pulmonary vascular tree, (iii) a quantitative view of structure based on morphometry of the vascular wall, (iv) the relationship of nerves, a variety of interstitial cells, matrix proteins, and striated myocytes to smooth muscle and endothelium in the vascular wall, (v) heterogeneity within cell populations and between vascular compartments, (vi) homo- and heterotypic cell-cell junctional complexes, and (vii) the relation of the pulmonary vasculature to that of airways. These issues for pulmonary vascular structure are compared, when data is available, across species from human to mouse and shrew. Data from studies utilizing vascular casting, light and electron microscopy, as well as models developed from those data, are discussed. Finally, the need for rigorous quantitative approaches to study of vascular structure in lung is highlighted.

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Structure and Composition of Pulmonary Arteries, Capillaries, and Veins

https://escholarship.org/content/qt09t1d4tb/qt09t1d4tb.pdf?t=q9hxlg

The Cellular and Physiological Basis for Lung Repair and Regeneration: Past, Present, and Future.

Small airways disease in mild and moderate chronic obstructive pulmonary disease: a cross-sectional study

The major function of the lung is gas exchange and depends on alveolar and capillary parameters such as surface area and volume. The number of alveoli may report on the nature of structural changes in lung parenchyma during development, illness or changing environmental factors. We therefore developed an efficient and easily applicable stereological design for estimating and monitoring these structural parameters in the mouse lung. The estimation of volume fractions of different lung compartments has been carried out by point counting. A combination of cycloid grids superimposed on vertical sections was used to estimate the capillary surface area with isotropic test lines. Capillary length could be measured using the harmonic mean of the surface weighted diameter. The Euler characteristic applied in the physical fractionator with varying but known sampling fractions (Horovitz-Thompson estimator) enabled us to estimate alveolar number. In adult mice lungs, we obtained total values for alveolar number of 2.31 x 10(6) alveoli in a pair of lungs, alveolar surface area of 82.2 cm(2), capillary surface area of 124 cm(2), and capillary length of 1.13 km. All values are corrected for tissue shrinkage. With this study we present a highly efficient combination of several design-based stereological tools for the unbiased estimation of alveolar number and volume as well as length, surface area, and diameter of capillaries in the mice lung. Anat Rec, 292:113-122, 2009. (c) 2008 Wiley-Liss, Inc.

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ar.20747

Juliane Knust

Papers

Stereological estimates of alveolar number and size and capillary length and surface area in mice lungs.