Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Supplementary Figure 5 | Respiratory Research

Supplementary Figure 5

From: Fibroblasts and monocyte macrophages contract and degrade three-dimensional collagen gels in extended co-culture

Supplementary Figure 5

Effect of varying cell number on gel contraction and collagen degradation. Collagen gels were prepared with co cultures containing varying concentrations of either monocytes or fibroblasts. The gels were then floated in either serum-free DMEM (panels a and c) or in medium containing human neutrophil elastase (NE) (panels b and d). After 4 days, the gel area (panels a and b) and hydroxyproline content (panels c and d) were determined. Panels a and b: vertical axes = gel size on day 4 (% of initial area). Panels c and d: vertical axes = hydroxyproline content in the gels (μg/gel). Horizontal axes: fibroblast and monocyte densities (105/ml). The data shown are means ± SEM for triplicate determinations from a representative single experiment. BM, blood monocytes; HFL, human lung fibroblasts. *P < 0.05, **P < 0.01 compared to monocytes alone. #P < 0.05, ##P < 0.01 compared to fibroblasts alone.

Back to article page