LAMP proteins are required for fusion of lysosomes with phagosomes
By K. Huynh, E. Eskelinen, Cameron C Scott, A. Malevanets, P. Saftig, S. Grinstein. EMBO Journal, 2007
686 citations recorded by the source corpus.
Subfields: Cell Biology, Epidemiology, Physiology
View Paper: https://www.semanticscholar.org/paper/c317aaf8f010019814010e41c2cff67305410e0b
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Citations in the corpus
- Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function (2009, background): “The significance of the intracellular localization of LAMPs is further exemplified by the observation that in LAMP-deficient cells the distribution of lysosomes is more dispersed and peripheral, suggesting that lysosome migration towards the microtubule organization centre is delaye”
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (2012, positive): “involved in the fusion of late endosomes and autophagosomes or phagosomes.(1118,1119) LAMP2C, one of the LAMP2 isoforms, can also function as an RNA/DNA receptor in RNautophagy”
- Lysosomes: fusion and function (2007, background): “Cells that are depleted of lysosomal-associated membrane protein-1 (LAMP1) and LAMP2 show abnormal phagosome maturatio”
- Autophagy: a lysosomal degradation pathway with a central role in health and disease. (2009, background): “Thematuration block caused by LAMP deficiency is at least partially due to the inability of autophagosomes and phagosomes to undergo dynein/dynactinmediated centripetal movement along microtubules towards lysosomes [158].”