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Human leukemic (HMC-1) mast cells are responsive to 1alpha, 25-dihydroxyvitamin D(3): selective promotion of ICAM-3 expression and constitutive presence of vitamin D(3) receptor.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2000 Jul 14; Vol. 273 (3), pp. 1104-10. - Publication Year :
- 2000
-
Abstract
- Expression levels of adhesion molecules on HMC-1 mast cells were examined prior to and following administration of 1alpha, 25-dihydroxyvitamin D(3) [1,25(OH)(2)D(3)]. While most receptors (including ICAM-1) remained unchanged by the treatment, solely ICAM-3 expression was promoted in a dose- and time-dependent fashion, peaking at 50 nM of 1,25(OH)(2)D(3) and 72 h, illustrating that like other myeloid cells, human mast cells are 1,25(OH)(2)D(3) responsive, yet in a highly selective manner. Flow cytometric results were confirmed by ELISA, by semiquantitative RT-PCR, and functionally by showing enhanced anti-ICAM-3 mediated homotypic aggregation of 1,25(OH)(2)D(3) pretreated cells. Since cellular responsiveness is conferred by the vitamin D(3) receptor (VDR), we examined human mast cells for its expression. VDR was constitutively present in both HMC-1 and skin mast cells by RT-PCR technique and in nuclear extracts of HMC-1 cells by Western blot analysis. Our data thus suggest that human mast cells are direct targets of 1, 25(OH)(2)D(3) action.<br /> (Copyright 2000 Academic Press.)
- Subjects :
- Base Sequence
DNA Primers
Enzyme-Linked Immunosorbent Assay
Humans
Leukemia metabolism
Mast Cells metabolism
Skin cytology
Skin metabolism
Antigens, CD
Antigens, Differentiation
Calcitriol pharmacology
Cell Adhesion Molecules metabolism
Leukemia pathology
Mast Cells drug effects
Receptors, Calcitriol metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 273
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 10891379
- Full Text :
- https://doi.org/10.1006/bbrc.2000.3083