The Second Extracellular Loop of CXCR4 Determines Its Function as a Receptor for Feline Immunodeficiency Virus

The feline homolog of the α-chemokine receptor CXCR4 has recently been shown to support cell-cell fusion mediated by CXCR4-dependent strains of human immunodeficiency virus (HIV) and strains of feline immunodeficiency virus (FIV) that have been selected for growth in the Crandell feline kidney (CrFK) cell line. In this report we demonstrate that expression of CXCR4 alone is sufficient to render cells from diverse species permissive for fusion with FIV-infected cells, suggesting that CXCR4 is the sole receptor for CrFK-tropic strains of FIV, analogous to CD4-independent strains of HIV-2. To identify the regions of CXCR4 involved in fusion mediated by FIV, we screened panels of chimeric CXCR4 molecules for the ability to support fusion with FIV-infected cells. Human CXCR4 supported fusion more efficiently than feline CXCR4 and feline/human CXCR4 chimeras, suggesting that the second and third extracellular loops of human CXCR4 contain a critical determinant for receptor function. Rat/human CXCR4 chimeras suggested that the second extracellular loop contained the principal determinant for receptor function; however, chimeras constructed between human CXCR2 and CXCR4 revealed that the first and third loops of CXCR4 contribute to the FIV Env binding site, as replacement of these domains with the corresponding domains of CXCR2 rendered the molecule nonfunctional in fusion assays. Mutation of the DRY motif and the C-terminal cytoplasmic tail of CXCR4 did not affect the ability of the molecule to support fusion, suggesting that neither signalling via G proteins nor receptor internalization was required for fusion mediated by FIV; similarly, truncation of the N terminus of CXCR4 did not affect the function of the molecule as a receptor for FIV. CXCR4-transfected feline cells were rendered permissive for infection with both the CrFK-tropic PET isolate of FIV and the CXCR4-dependent RF strain of HIV-1, and susceptibility to infection correlated well with ability to support fusion. The data suggest that the second extracellular loop of CXCR4 is the major determinant of CXCR4 usage by FIV.     

Vaccine-specific local T cell reactivity in immunotherapy-associated vitiligo in melanoma patients

The occurrence of vitiligo in patients with melanoma is especially reported for patients undergoing immunotherapy. While vitiligo in these patients is thought to be related to an immune response directed against melanoma cells, solid evidence is lacking. Here we report local cytotoxic T cell reactivity in three melanoma patients who developed vitiligo, after experimental immunotherapy using dendritic cell vaccinations. Tetramer analysis showed that vaccine-induced T cells recognizing gp100 and tyrosinase are present at the vitiligo lesions. These T cells secrete IFN-γ and IL-2 upon peptide specific stimulation as well as upon recognition of the autologous tumor. We show that functional CD8⁺ T cells specific for melanoma differentiation antigens used in a melanoma immunotherapy trial, do not only invade the tumor, but also the vitiligo lesions. This directly links vitiligo to the immuno-therapeutic intervention and supports the hypothesis that vitiligo is a marker of immunity against melanoma cells. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Possible positive-feedback mechanisms: plants change abiotic soil parameters in wet calcareous dune slacks

In this paper the results are presented from a mesocosm study of the effects of typical dune slack plants on the soil solution nutrient contents. In dune slack succession, early successional species often show radial oxygen loss (ROL) whereas their successor species do not show ROL. ROL has impact on abiotic soil parameters and therefore, affect the competitiveness of both species. Mesocosms with Littorella uniflora and Carex nigra, used as respectively a ROL and a non-ROL species, showed remarkable differences in soil solution parameters. Special attention was given to nitrogen, as it is the limiting resource in dune slack succession. Mesocosms with L. uniflora showed a higher nitrate content in the soil than mesocosms with C. nigra and the control. Moreover, estimating the nitrogen balance, a significantly higher fraction of nitrogen was missing in L. uniflora (57%) than in C. nigra (5%). The enhanced nitrogen loss in mesocosms with L. uniflora could act as a positive-feedback mechanism for early successional stages that slows down the vegetation development in early stages of dune slack succession towards the more-productive later stages. The mechanism could even lead to alternative stable states in dune slack succession.     

MalariaSphere: A greenhouse-enclosed simulation of a natural Anopheles gambiae (Diptera: Culicidae) ecosystem in western Kenya

Background  

The development and implementation of innovative vector control strategies for malaria control in Africa requires in-depth ecological studies in contained semi-field environments. This particularly applies to the development and release of genetically-engineered vectors that are refractory to Plasmodium infection. Here we describe a modified greenhouse, designed to simulate a natural Anopheles gambiae Giles ecosystem, and the first successful trials to complete the life-cycle of this mosquito vector therein.     

Effects of microbial mats on germination and seedling survival of typical dune slack species in the Netherlands

The role of microbial mats in wet dune slack succession is often discussed. We tested if presence of microbial mats may retard dune slack succession by lowering the germination and seeding survival of successor species. This hypothesis was tested on a set of typical dune slack species of the Frisian Islands in two climate chamber experiments. The species were separated into early-, intermediate- and late successional species. There were large differences in germination rates between species (2% – >200% compared to the reference), but within a species the high germination rates were mostly found on sand without a microbial mat. Only the germination of Agrostis stolonifera appeared to be stimulated by the presence of a well-developed microbial mat, they were even higher than in the reference. Seedling survival also did not show different responses between successional stages. Seedlings placed on top of a microbial mat showed for most species lower survival rates compared to seedlings that were planted or placed on top of the sand. Growth was the only measured variable that differed between successional groups. Species of the early- and intermediate successional stages grew significantly better if a microbial mat was present whereas late successional species were not stimulated. Early and intermediate successional species seem to be favored by the presence of a microbial mat. An explanation for this may be that they can profit from the enhanced nitrogen availability caused by N₂-fixation by cyanobacteria in the microbial mat. This revised version was published online in June 2006 with corrections to the Cover Date.     

The dendritic cell-specific CC-chemokine DC-CK1 is expressed by germinal center dendritic cells and attracts CD38-negative mantle zone B lymphocytes

DC-CK1 (CCL18) is a dendritic cell (DC)-specific chemokine expressed in both T and B cell areas of secondary lymphoid organs that preferentially attracts CD45RA(+) T cells. In this study, we further explored the nature of DC-CK1 expressing cells in germinal centers (GCs) of secondary lymphoid organs using a newly developed anti-DC-CK1 mAb. Immunohistochemical analysis demonstrated a remarkable difference in the number of DC-CK1 expressing cells in adjacent GCs within one tonsil, implicating that the expression of DC-CK1 in GCs depends on the activation and/or progression stage of the GC reaction. Using immunohistology and RNA analysis, we demonstrated that GCDC are the source of DC-CK1 production in the GCs. Considering the recently described function of GCDC in (naive) B cell proliferation, isotype switching and Ab production, we investigated the ability of DC-CK1 to attract B lymphocytes. Here we demonstrate that DC-CK1 is a pertussis toxin-dependent chemoattractant for B lymphocytes with a preference in attracting mantle zone (CD38(-)) B cells. The findings that GCDC produce DC-CK1 and attract mantle zone B cells support a key role for GCDC in the development of GCs and memory B cell formation.