Publications by authors named "D I Jarmin"

Article Synopsis
  • Researchers found that the beta-chemokine ESkine/CCL27 has two forms: a secreted version (ESkine) and a nuclear-targeted version (PESKY) that lacks a signal peptide.
  • * The study identified that PESKY's movement into the nucleus depends on specific C-terminal residues, which are also present in ESkine, suggesting both can enter the nucleus through a similar mechanism.
  • * Overexpression of PESKY in cells led to significant changes in the actin cytoskeleton and increased cell migration, indicating a possible new role for these chemokines in cellular movement and structure.*
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A number of orphan G-protein coupled receptors (GPR) have been reported as putative chemokine receptors. One previously reported orphan receptor is an incomplete PCR clone, called GPR2. Here we report the cloning of full-length human (h)GPR2 and mouse (m)GPR2 cDNAs, and the identification of GPR2 as a receptor for a novel CC chemokine called ESkine.

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The beta-chemokine macrophage inflammatory protein-1 alpha (MIP-1alpha) and its associated receptors are involved in the regulation of pro-inflammatory and haemopoietic processes. This study was designed to investigate regulation of expression MIP-1alpha and its receptors by other haemopoietic cytokines. Murine bone marrow macrophages (BMM) were treated with or without GM-CSF or IL-3 and expression of MIP-1alpha, other chemokines and their receptors examined by Northern blotting.

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Mast cells are an important source of a number of lymphokines and chemokines primarily those released after challenge with the allergic trigger IgE and Ag. However, the mechanisms of lymphokine and chemokine gene activation in this cell type, as opposed to the mechanisms of activation in T cells, are poorly understood. As a model system, we addressed this issue in mast cells by using the recently cloned chemokine MARC gene, which belongs to the RANTES/sis gene family.

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