LAMP proteins are required for fusion of lysosomes with phagosomes

Abstract

Lysosome‐associated membrane proteins 1 and 2 (LAMP‐1 and LAMP‐2) are delivered to phagosomes during the maturation process. We used cells from LAMP‐deficient mice to analyze the role of these proteins in phagosome maturation. Macrophages from LAMP‐1‐ or LAMP‐2‐deficient mice displayed normal fusion of lysosomes with phagosomes. Because ablation of both the lamp‐1 and lamp‐2 genes yields an embryonic‐lethal phenotype, we were unable to study macrophages from double knockouts. Instead, we reconstituted phagocytosis in murine embryonic fibroblasts (MEFs) by transfection of FcγIIA receptors. Phagosomes formed by FcγIIA‐transfected MEFs obtained from LAMP‐1‐ or LAMP‐2‐ deficient mice acquired lysosomal markers. Remarkably, although FcγIIA‐transfected MEFs from double‐deficient mice ingested particles normally, phagosomal maturation was arrested. LAMP‐1 and LAMP‐2 double‐deficient phagosomes acquired Rab5 and accumulated phosphatidylinositol 3‐phosphate, but failed to recruit Rab7 and did not fuse with lysosomes. We attribute the deficiency to impaired organellar motility along microtubules. Time‐lapse cinematography revealed that late endosomes/lysosomes as well as phagosomes lacking LAMP‐1 and LAMP‐2 had reduced ability to move toward the microtubule‐organizing center, likely precluding their interaction with each other.