Calcitonin receptor-like receptor is expressed on gastrointestinal immune cells
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vor 22 Jahren
Background/Aims: Pharmacological and morphological studies suggest
that the gut mucosal immune system and local
neuropeptide-containing neurones interact. We aimed to determine
whether gut immune cells are targets for calcitonin gene-related
peptide (CGRP), which has potent immune regulatory properties.
Methods: Using density gradient centrifugation, rat lamina propria
mononuclear cells (LP-MNCs) and intra-epithelial lymphocytes (IELs)
were isolated. RT-PCR was employed for the detection of mRNA of rat
calcitonin receptor-like receptor (CRLR), which is considered to
represent the pharmacologically defined CGRP receptor-1 subtype, as
well as mRNA of the receptor activity-modifying proteins, which are
essential for CRLR function and determine ligand specificity. A
radioreceptor assay was employed for the detection of specific CGRP
binding sites. Results: RT-PCR and DNA sequencing showed that
LP-MNCs and IELs express CRLR. Incubation of isolated LP-MNCs with
radiolabelled alphaCGRP revealed the existence of specific binding
sites for CGRP. Conclusion: These novel data indicate that mucosal
immune cells of the rat gut are a target for CGRP and provide
significant evidence that CGRP functions as an immune regulator in
the gut mucosa. Copyright (C) 2002 S. Karger AG, Basel.
that the gut mucosal immune system and local
neuropeptide-containing neurones interact. We aimed to determine
whether gut immune cells are targets for calcitonin gene-related
peptide (CGRP), which has potent immune regulatory properties.
Methods: Using density gradient centrifugation, rat lamina propria
mononuclear cells (LP-MNCs) and intra-epithelial lymphocytes (IELs)
were isolated. RT-PCR was employed for the detection of mRNA of rat
calcitonin receptor-like receptor (CRLR), which is considered to
represent the pharmacologically defined CGRP receptor-1 subtype, as
well as mRNA of the receptor activity-modifying proteins, which are
essential for CRLR function and determine ligand specificity. A
radioreceptor assay was employed for the detection of specific CGRP
binding sites. Results: RT-PCR and DNA sequencing showed that
LP-MNCs and IELs express CRLR. Incubation of isolated LP-MNCs with
radiolabelled alphaCGRP revealed the existence of specific binding
sites for CGRP. Conclusion: These novel data indicate that mucosal
immune cells of the rat gut are a target for CGRP and provide
significant evidence that CGRP functions as an immune regulator in
the gut mucosa. Copyright (C) 2002 S. Karger AG, Basel.
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