Published online before print December 15, 2004
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* Departments of Tumor Immunology and
Cell Biology, Nijmegen Center for Molecular Life Sciences, University Medical Center Nijmegen, The Netherlands; and
Crucell Leiden, The Netherlands
1 Correspondence: Department of Tumor Immunology, NCMLS/187 TIL University Medical Center, Postbox 9101, 6500HB Nijmegen, The Netherlands. E-mail: g.adema{at}ncmls.kun.nl
Recently, we described the molecular identification of dendritic cell-specific TrAnsMembrane protein (DC-STAMP), a multimembrane-spanning protein preferentially expressed by human DC (hDC). In this report, we describe the identification and expression profile of the murine homologue of DC-STAMP (mDC-STAMP) as well as the characterization of the DC-STAMP protein. The results demonstrate that mDC-STAMP is over 90% homologous to hDC-STAMP and is also preferentially expressed by DC in vitro and ex vivo. mDC-STAMP expression is enhanced by interleukin-4 and down-regulated upon DC maturation. Analysis of differently tagged DC-STAMP proteins further demonstrates that hDC-STAMP and mDC-STAMP are glycosylated and primarily localize to an intracellular compartment. Applying confocal microscopy and electron microscopy, we demonstrate that hDC-STAMP localizes to the endoplasmic reticulum (ER) in human embryonic kidney 293 cells as well as hDC transduced with an adenovirus encoding hDC-STAMP-green fluorescent protein fusion protein. These data imply that DC-STAMP may exert its effect in the ER.
Key Words: mouse human APC CLSM immunobiology
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