Cited by 29Mast cells and histamineChemokine receptors and signalingAsthma and respiratory diseases

Progesterone reduces the migration of mast cells toward the chemokine stromal cell-derived factor-1/CXCL12 with an accompanying decrease in CXCR4 receptors.

Belot, Marie-Pierre, Abdennebi-Najar, Latifa, Gaudin, Françoise, Lieberherr, Michèle, Godot, Véronique, Taïeb, Joelle, Emilie, Dominique, Machelon, Véronique·2007·American Journal of Physiology-Endocrinology and Metabolism

Abstract

Mast cell recruitment is implicated in many physiological functions and several diseases. It depends on microenvironmental factors, including hormones. We have investigated the effect of progesterone on the migration of HMC-1(560) mast cells toward CXCL12, a chemokine that controls the migration of mast cells into tissues. HMC-1(560) mast cells were incubated with 1 nM to 1 microM progesterone for 24 h. Controls were run without progesterone. Cell migration toward CXCL12 was monitored with an in vitro assay, and statistical analysis of repeated experiments revealed that progesterone significantly reduced cell migration without increasing the number of apoptotic cells (P = 0.0084, n = 7). Differences between progesterone-treated and untreated cells were significant at 1 microM (P < 0.01, n = 7). Cells incubated with 1 microM progesterone showed no rearrangment of actin filaments in response to CXCL12. Progesterone also reduced the calcium response to CXCL12 and Akt phosphorylation. Cells incubated with progesterone had one-half the control concentrations of CXCR4 (mRNA, total protein, and membrane-bound protein). Progesterone also inhibited the migration of HMC-1(560) cells transfected with hPR-B-pSG5 plasmid, which contained 2.5 times as much PR-B as the control. These transfected cells responded differently (P < 0.05, n = 5) from untreated cells to 1 nM progesterone. We conclude that progesterone reduces mast cell migration toward CXCL12 and that CXCR4 may be a progesterone target in mast cells.

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Crossref · 10.1152/ajpendo.00286.2006

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Authors
Belot, M.-P., Abdennebi-Najar, L., Gaudin, F., Lieberherr, M., Godot, V., Taïeb, J., Emilie, D., & Machelon, V.
Affiliations
Inserm (FR)
Venue
American Journal of Physiology-Endocrinology and Metabolism
Published
2007-05
Volume
292
Issue
5
Pages
E1410-E1417
ISSN
  • 0193-1849 (ISSN-L)
  • 1522-1555
OpenAlex
W2167932732
Cited by
29
References
50
Citations by year
2023: 1 · 2022: 2 · 2021: 2 · 2020: 2 · 2019: 1 · 2016: 3 · 2015: 3 · 2012: 3
FWCI
1.36
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
Funders
Institut National de la Santé et de la Recherche Médicale
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
  • Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
  • Health Sciences › Medicine › Physiology › Asthma and respiratory diseases
Keywords
progesterone, mast cell migration, CXCL12, CXCR4, progesterone receptor B, chemokine signaling, calcium response, Akt phosphorylation, actin cytoskeleton, mast cell recruitment
MeSH terms
Wortmannin, Actins, Androstadienes, Calcium, Cell Movement, Flow Cytometry, Humans, Mast Cells, Phosphorylation, Progesterone, Receptors, Progesterone, RNA, Messenger, Blotting, Western, Receptors, CXCR4, Chemokines, CXC, Reverse Transcriptase Polymerase Chain Reaction, Protein Kinase Inhibitors, Oncogene Protein v-akt, Chemokine CXCL12

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