Literature DB >> 14764901

Development of a specific system for targeting protein to metallophilic macrophages.

Philip R Taylor1, Susanne Zamze, Richard J Stillion, Simon Y C Wong, Siamon Gordon, Luisa Martinez-Pomares.   

Abstract

The cysteine-rich domain (CR) of the mannose receptor binds sulfated glycoprotein CR ligand (CRL) expressed by subpopulations of myeloid cells in secondary lymphoid organs (CRL(+) cells). In naïve mice, these CRL(+) cells, metallophilic macrophages (M) in spleen and subcapsular sinus M in lymph nodes, are located strategically for antigen capture and are adjacent to B cell follicles, but their role in the immune response is unknown. We have exploited the lectin activity of CR to develop a highly specific system for targeting protein to CRL(+) M. We demonstrate that the sulfated carbohydrates recognized by CR are exposed to the extracellular milieu and mediate highly specific targeting of CR-containing proteins. This model will allow the dissection of the role of metallophilic M in an immune response in vivo.

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Year:  2004        PMID: 14764901      PMCID: PMC357035          DOI: 10.1073/pnas.0308490100

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  19 in total

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4.  The differential effects of bacterial lipopolysaccharide (LPS) on splenic non-lymphoid cells demonstrated by monoclonal antibodies.

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6.  Mannose receptor ligand-positive cells express the metalloprotease decysin in the B cell follicle.

Authors:  C G Mueller; I Cremer; P E Paulet; S Niida; N Maeda; S Lebeque; W H Fridman; C Sautès-Fridman
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7.  Analysis of mannose receptor regulation by IL-4, IL-10, and proteolytic processing using novel monoclonal antibodies.

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8.  In-vivo effects of lipopolysaccharide on lymphoid and non-lymphoid cells in the mouse spleen. Migration of marginal metallophils towards the follicle centres.

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6.  Altered expression and endocytic function of CD205 in human dendritic cells, and detection of a CD205-DCL-1 fusion protein upon dendritic cell maturation.

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