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Mice Lacking Platelet-Derived Growth Factor D Display a Mild Vascular Phenotype
Hanna Gladh1, Erika Bergsten Folestad1, Lars Muhl1
1Department of Medical Biochemistry and Biophysics, Division of Vascular Biology, Karolinska Institutet, Stockholm, Sweden.
Plos One
|April 1, 2016
Summary
Platelet-derived growth factor D (PDGF-D) knockout mice showed mild vascular defects and slightly increased blood pressure, suggesting PDGF-D's role in vascular homeostasis.
Area of Science:
- Vascular Biology
- Developmental Biology
- Genetics
Background:
- Platelet-derived growth factor D (PDGF-D) is the newest member of the PDGF family, with largely unknown biological functions.
- Unlike other PDGFs, PDGF-D has not been studied using gene inactivation in mice.
Purpose of the Study:
- To characterize the biological role of PDGF-D by creating and analyzing a constitutive Pdgfd knockout mouse model.
- To investigate the expression pattern and function of PDGF-D in vivo.
Main Methods:
- Generation of a constitutive Pdgfd knockout mouse model (Pdgfd-/-) with a LacZ reporter.
- Phenotypic analysis of Pdgfd-/- mice, including viability, fertility, and health assessment.
- Localization of Pdgfd promoter activity using the LacZ reporter in various tissues.
- Assessment of vascular structure, specifically NG2-expressing pericytes, and blood pressure measurements.
Main Results:
- Pdgfd knockout mice exhibited a mild phenotype, with viable and fertile offspring.
- Pdgfd expression was primarily observed in vascular structures, particularly in arteries and bifurcations, with endothelial cells as the main source.
- Disorganization of NG2-expressing pericytes in cardiac vasculature and a slight elevation in blood pressure were noted in Pdgfd-/- mice.
Conclusions:
- PDGF-D plays a role in regulating systemic arterial blood pressure.
- The findings suggest PDGF-D is involved in maintaining vascular homeostasis, particularly in arterial structures and associated mural cells.

