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Huixing Wu, Alexander Kuzmenko, Sijue Wan, Lyndsay Schaffer, Alison Weiss, James H. Fisher, Kwang Sik Kim, Francis X. McCormack
Published in Volume 111, Issue 10
J Clin Invest. 2003; 111(10):1589–1602 doi:10.1172/JCI16889
Abstract | Full text | PDF
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Figure 5

Attenuation of E. coli K12–induced light scattering by SP-A and SP-D. (a) E. coli K12 were mixed with 25 μg/ml (open squares) or 250 μg/ml (open triangles) hSP-A or no protein (open circles) and incubated in LB at 37°C in a shaking water bath. Bacterial density was monitored by absorbance at 400 nm. (b) E. coli grown as above were incubated with hSP-A (filled circles), 300 μg/ml J5 LPS (open circles), 300 μg/ml J5 LPS plus 100 μg/ml hSP-A (open triangles), or no additives (x’s). (c) E. coli grown as above were incubated with 100 μg/ml rmSP-D (open squares), 300 μg/ml J5 LPS (open triangles), or 300 μg/ml J5 LPS plus 100 μg/ml rmSP-D (filled circles). Data are mean ± SEM; n = 3. (d) Bacterial aggregation was assessed under the light microscope after incubation of E. coli K12 with hSP-A, rSP-A, rrSP-A, a C-terminal fragment of SP-A containing residues A81–F228 (ΔSP-A), rSP-D, rmSP-D, a C-terminal fragment of SP-D containing residues D203–F355 (ΔSP-D), or BSA, and viewed with the light microscope.