TY - JOUR
T1 - LC3-associated phagocytosis
T2 - host defense and microbial response
AU - Upadhyay, Sandeep
AU - Philips, Jennifer A.
N1 - Funding Information:
We thank Milan G. Chheda for his comments on the manuscript. This work was supported by the National Institutes of Health (R01 AI130454) and Washington University School of Medicine.
Funding Information:
We thank Milan G. Chheda for his comments on the manuscript. This work was supported by the National Institutes of Health ( R01 AI130454 ) and Washington University School of Medicine .
Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/10
Y1 - 2019/10
N2 - The innate immune system has evolved to recognize diverse microbes and destroy them. At the same time, microbial pathogens undermine immunity to cause disease. Here, we highlight recent advances in understanding an antimicrobial pathway called LC3-associated phagocytosis (LAP), which combines features of autophagy with phagocytosis. Upon phagocytosis, many microbes, including bacteria, fungi, and parasites, are sequestered in an LC3-positive, single-membrane bound compartment, a hallmark of LAP. LAP depends upon NADPH oxidase activity at the incipient phagosome and culminates in lysosomal trafficking and microbial degradation. Most often LAP is an effective host defense, but some pathogens evade LAP or replicate successfully in this microenvironment. Here, we review how LAP targets microbial pathogens and strategies pathogens employ to circumvent LAP.
AB - The innate immune system has evolved to recognize diverse microbes and destroy them. At the same time, microbial pathogens undermine immunity to cause disease. Here, we highlight recent advances in understanding an antimicrobial pathway called LC3-associated phagocytosis (LAP), which combines features of autophagy with phagocytosis. Upon phagocytosis, many microbes, including bacteria, fungi, and parasites, are sequestered in an LC3-positive, single-membrane bound compartment, a hallmark of LAP. LAP depends upon NADPH oxidase activity at the incipient phagosome and culminates in lysosomal trafficking and microbial degradation. Most often LAP is an effective host defense, but some pathogens evade LAP or replicate successfully in this microenvironment. Here, we review how LAP targets microbial pathogens and strategies pathogens employ to circumvent LAP.
UR - http://www.scopus.com/inward/record.url?scp=85067632767&partnerID=8YFLogxK
U2 - 10.1016/j.coi.2019.04.012
DO - 10.1016/j.coi.2019.04.012
M3 - Review article
C2 - 31247378
AN - SCOPUS:85067632767
SN - 0952-7915
VL - 60
SP - 81
EP - 90
JO - Current Opinion in Immunology
JF - Current Opinion in Immunology
ER -