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J Appl Physiol 98: 672-679, 2005. First published September 24, 2004; doi:10.1152/japplphysiol.00619.2004
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Mechanical interactions between collagen and proteoglycans: implications for the stability of lung tissue

Francisco S. A. Cavalcante,1,2,3 Satoru Ito,2 Kelly Brewer,2 Hiroaki Sakai,2 Adriano M. Alencar,2 Murilo P. Almeida,3 José S. Andrade, Jr.,3 Arnab Majumdar,2 Edward P. Ingenito,4 and Béla Suki2

1Department of Física e Química, Universidade Estadual do Ceará, Fortaleza; 2Department of Biomedical Engineering, Boston University, Boston; 3Department of Física, Universidade Federal do Ceará, Fortaleza, Ceará, Brazil; and 4Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts

Submitted 18 June 2004 ; accepted in final form 23 August 2004

Collagen and elastin are thought to dominate the elasticity of the connective tissue including lung parenchyma. The glycosaminoglycans on the proteoglycans may also play a role because osmolarity of interstitial fluid can alter the repulsive forces on the negatively charged glycosaminoglycans, allowing them to collapse or inflate, which can affect the stretching and folding pattern of the fibers. Hence, we hypothesized that the elasticity of lung tissue arises primarily from 1) the topology of the collagen-elastin network and 2) the mechanical interaction between proteoglycans and fibers. We measured the quasi-static, uniaxial stress-strain curves of lung tissue sheets in hypotonic, normal, and hypertonic solutions. We found that the stress-strain curve was sensitive to osmolarity, but this sensitivity decreased after proteoglycan digestion. Images of immunofluorescently labeled collagen networks showed that the fibers follow the alveolar walls that form a hexagonal-like structure. Despite the large heterogeneity, the aspect ratio of the hexagons at 30% uniaxial strain increased linearly with osmolarity. We developed a two-dimensional hexagonal network model of the alveolar structure incorporating the mechanical properties of the collagen-elastin fibers and their interaction with proteoglycans. The model accounted for the stress-strain curves observed under all experimental conditions. The model also predicted how aspect ratio changed with osmolarity and strain, which allowed us to estimate the Young's modulus of a single alveolar wall and a collagen fiber. We therefore identify a novel and important role for the proteoglycans: they stabilize the collagen-elastin network of connective tissues and contribute to lung elasticity and alveolar stability at low to medium lung volumes.

glycosaminoglycans; stress-strain; stiffness; fluorescent imaging; network



Address for reprint requests and other correspondence: B. Suki, Dept. of Biomedical Engineering, Boston Univ., 44 Cummington St., Boston, MA 02215 (E-mail: bsuki{at}bu.edu)




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