Macrosialin, a macrophage-restricted membrane sialoprotein differentially glycosylated in response to inflammatory stimuli
- PMID: 1919437
- PMCID: PMC2118958
- DOI: 10.1084/jem.174.4.827
Macrosialin, a macrophage-restricted membrane sialoprotein differentially glycosylated in response to inflammatory stimuli
Erratum in
- J Exp Med 1992 Jan 1;175(1):309
Abstract
Rat monoclonal antibody FA/11 has been used to identify macrosialin, a sialoglycoprotein confined to murine mononuclear phagocytes and related cells. Originally identified as a macrophage-associated glycoprotein predominantly localized in intracellular membranes (Smith, M.J., and G.L.E. Koch. 1987. J. Cell Sci. 87:113), the antigen is widely expressed on tissue macrophages, including those in lymphoid areas, and is expressed at low levels on isolated dendritic cells. Immuno-adsorption experiments reported here show that macrosialin is identical to the major 87-115-kD sialoglycoprotein previously identified by lectin blotting in exudate but not resident peritoneal macrophages (Rabinowitz, S., and S. Gordon. 1989. J. Cell Sci. 93:623). Resident peritoneal macrophages express low levels of macrosialin antigen in a glycoform that does not bind 125I wheat germ agglutinin or 125I peanut agglutinin; inflammatory stimuli upregulate expression of this antigen (up to 17-fold), in an alternative glycoform that is detected by these lectins. Pulse-chase experiments reveal a 44-kD core peptide that initially bears high-mannose chains (giving Mr 66 kD) and is subsequently processed to a mature protein of Mr 87-104 kD. Each glycoform contains N-linked glycan, as well as O-linked sugar structures that show alternative processing. Poly-N-acetyllactosamine structures are detected in the exudate cell glycoform only. This new marker for mononuclear phagocytes illustrates two strategies by which macrophages remodel their membranes in response to inflammatory stimuli. Its predominantly intracellular location and restricted cell distribution suggest a possible role in membrane fusion or antigen processing.
Similar articles
-
Differential expression of membrane sialoglycoproteins in exudate and resident mouse peritoneal macrophages.J Cell Sci. 1989 Aug;93 ( Pt 4):623-30. doi: 10.1242/jcs.93.4.623. J Cell Sci. 1989. PMID: 2606943
-
Macrosialin, a mouse macrophage-restricted glycoprotein, is a member of the lamp/lgp family.J Biol Chem. 1993 May 5;268(13):9661-6. J Biol Chem. 1993. PMID: 8486654
-
Human monocyte-derived macrophages express an approximately 120-kD Ox-LDL binding protein with strong identity to CD68.Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):3107-16. doi: 10.1161/01.atv.17.11.3107. Arterioscler Thromb Vasc Biol. 1997. PMID: 9409300
-
Phagocytosis stimulates alternative glycosylation of macrosialin (mouse CD68), a macrophage-specific endosomal protein.Biochem J. 1999 Mar 15;338 ( Pt 3)(Pt 3):687-94. Biochem J. 1999. PMID: 10051440 Free PMC article.
-
Immunocytochemical characterization of the endocytic and phagolysosomal compartments in peritoneal macrophages.J Cell Biol. 1992 Jan;116(1):95-112. doi: 10.1083/jcb.116.1.95. J Cell Biol. 1992. PMID: 1730752 Free PMC article.
Cited by
-
The use of human CD68 transcriptional regulatory sequences to direct high-level expression of class A scavenger receptor in macrophages in vitro and in vivo.Immunology. 2001 Jul;103(3):351-61. doi: 10.1046/j.1365-2567.2001.01256.x. Immunology. 2001. PMID: 11454064 Free PMC article.
-
CD68/macrosialin: not just a histochemical marker.Lab Invest. 2017 Jan;97(1):4-13. doi: 10.1038/labinvest.2016.116. Epub 2016 Nov 21. Lab Invest. 2017. PMID: 27869795
-
Quetiapine Ameliorates MIA-Induced Impairment of Sensorimotor Gating: Focus on Neuron-Microglia Communication and the Inflammatory Response in the Frontal Cortex of Adult Offspring of Wistar Rats.Cells. 2022 Sep 7;11(18):2788. doi: 10.3390/cells11182788. Cells. 2022. PMID: 36139363 Free PMC article.
-
Phenotypic change of human cultured meningioma cells.J Neurooncol. 2000 Aug;49(1):9-17. doi: 10.1023/a:1006436903976. J Neurooncol. 2000. PMID: 11131990
-
Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis.Front Med (Lausanne). 2022 Dec 2;9:982399. doi: 10.3389/fmed.2022.982399. eCollection 2022. Front Med (Lausanne). 2022. PMID: 36530874 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous