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. 2008 Aug;49(8):1646–1657. doi: 10.1194/jlr.M700482-JLR200

Fig. 6.

Fig. 6.

Hematoxylin-eosin (H and E) staining of liver, spleen, and small intestine of wild-type, and PBS- or G-hLAL-treated lal−/− mice. Sections were from age-matched lal+/+ (A, D, G), lal−/− untreated mice (B, E, H), or G-hLAL-treated with 72 U (C, F, I). The lipid-laden Kupffer cells (B), spleen (E), and small intestine (H) macrophages were clearly evident in untreated lal−/− mice (arrows). Complete correction of lipid storage in macrophages (arrows in C, I) was observed in macrophages of these tissues of G-hLAL-treated mice. Hepatocytes was not corrected (arrowhead). Top row, liver (Kupffer cells); middle row, spleen; bottom row, small intestine.