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Human normal dermal fibroblasts express somatostatin receptors
A Gaudillère1, C Bernard, J Abello
1INSERM U346, E. Herriot Hospital, Lyon, France.
Experimental Dermatology
|August 10, 1999
Summary
Somatostatin receptors are present on human skin fibroblasts. These receptors, specifically subtype 2 or 3, can bind somatostatin and octreotide, with a weak impact on fibroblast DNA synthesis.
Area of Science:
- Endocrinology
- Dermatology
- Molecular Biology
Background:
- Somatostatin (SOM) is a hormone with diverse functions across multiple physiological systems.
- Endogenous SOM exists in 14- and 28-amino acid forms, interacting with five cloned receptor subtypes.
- Somatostatin and its receptors are present in human skin.
Purpose of the Study:
- To investigate the expression and characteristics of somatostatin receptors on normal human dermal fibroblasts.
- To determine the binding affinity and capacity of these receptors for somatostatin and related analogs.
- To evaluate the functional effect of somatostatin on fibroblast DNA synthesis.
Main Methods:
- Human dermal fibroblasts were utilized to study somatostatin receptor expression.
- Biotinyl-SOM was used for receptor visualization, and radioligand binding assays with (3-[125I]iodotyrosyl11)-SOM-14 were performed.
- DNA synthesis was assessed via [3H]-methyl thymidine incorporation, and competitive displacement studies were conducted.
Main Results:
- Saturation and Scatchard analyses revealed a homogeneous class of somatostatin receptors with a Bmax of 0.055 +/- 0.023 nM and KD of 2.0 +/- 0.4 nM.
- Human dermal fibroblasts possess approximately 3,317 +/- 1,385 binding sites per cell.
- Competitive binding assays indicated affinity for SOM-14, SOM-28, and octreotide, suggesting the presence of somatostatin receptor subtype 2 or 3.
Conclusions:
- Human normal dermal fibroblasts express somatostatin receptors, likely subtype 2 or 3.
- These receptors exhibit specific binding affinities for somatostatin and octreotide.
- Somatostatin showed a minimal effect on fibroblast DNA synthesis at the tested concentrations.