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- Zimmerli, StefanDivision of Infectious Diseases and The Rosalind Russell Arthritis Research Laboratory, San Francisco General Hospital, University of California at San Francisco, San Francisco, California, USA (författare)
Phagosome-Lysosome Fusion Is a Calcium-independent Event in Macrophages
- Artikel/kapitelEngelska1996
Förlag, utgivningsår, omfång ...
- 1996-01-01
- Rockefeller University Press,1996
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- LIBRIS-ID:oai:DiVA.org:liu-98037
- https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-98037URI
- https://doi.org/10.1083/jcb.132.1.49DOI
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- Språk:engelska
- Sammanfattning på:engelska
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- Phagosome-lysosome membrane fusion is a highly regulated event that is essential for intracellular killing of microorganisms, Functionally, it represents a form of polarized regulated secretion, which is classically dependent on increases in intracellular ionized calcium ([Ca2+](i)). Indeed, increases in [Ca2+](i) are essential for phagosome-granule (lysosome) fusion in neutrophils and for lysosomal fusion events that mediate host cell invasion by Trypanosoma cruzi trypomastigotes, Since several intracellular pathogens survive in macrophage phagosomes that do not fuse with lysosomes, we examined the regulation of phagosome-lysosome fusion in macrophages. Macrophages (MO) were treated with 12.5 mu M bis-(2-amino-S-methylphenoxy) ethane-N,N,N',N',-tetraacetic acid tetraacetoxymethyl ester (MAPT/AM), a cell-permeant calcium chelator which reduced resting cytoplasmic [Ca2+]; from 80 nM to less than or equal to 20 nM and completely blocked increases in [Ca2+](i) in response to multiple stimuli, even in the presence of extracellular calcium, Subsequently, MO phagocytosed serum-opsonized zymosan, staphylococci, or Mycobacterium bovis, Microbes were enumerated by 4',6-diamidino-2-phenylindole, dihydrochloride (DAPI) staining, and phagosome-lysosome fusion was scored using both lysosome-associated membrane protein (LAMP-1) as a membrane marker and rhodamine dextran as a content marker for lysosomes, Confirmation of phagosomelysosome fusion by electron microscopy validated the fluorescence microscopy findings, We found that phagosome-lysosome fusion in MO occurs normally at very low [Ca2+](i) (less than or equal to 20 nM), Kinetic analysis showed that in MO none of the steps leading from particle binding to eventual phagosome-lysosome fusion are regulated by [Ca2+](i) in a rate-limiting way. Furthermore, confocal microscopy revealed no difference in the intensity of LAMP-1 immunofluorescence in phagolysosome membranes in calcium-buffered vs, control macrophages, We conclude that neither membrane recognition nor fusion events in the phagosomal pathway in macrophages are dependent on or regulated by calcium.
Biuppslag (personer, institutioner, konferenser, titlar ...)
- Majeed, MeythamLinköpings universitet,Medicinsk mikrobiologi,Hälsouniversitetet(Swepub:liu)meyma63 (författare)
- Gustafsson, MikaelLinköpings universitet,Medicinsk mikrobiologi,Hälsouniversitetet(Swepub:liu)mikgu97 (författare)
- Stendahl, OlleLinköpings universitet,Medicinsk mikrobiologi,Hälsouniversitetet(Swepub:liu)ollst48 (författare)
- Sanan, David A.Gladstone Institute of Cardiovascular Disease, San Francisco, California, USA (författare)
- Ernst, Joel D.Division of Infectious Diseases and The Rosalind Russell Arthritis Research Laboratory, San Francisco General Hospital, University of California at San Francisco, San Francisco, California, USA (författare)
- Division of Infectious Diseases and The Rosalind Russell Arthritis Research Laboratory, San Francisco General Hospital, University of California at San Francisco, San Francisco, California, USAMedicinsk mikrobiologi (creator_code:org_t)
Sammanhörande titlar
- Ingår i:Journal of Cell Biology: Rockefeller University Press132:1-2, s. 49-610021-95251540-8140
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