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Updated: Jul 31, 2025

Fabricating a Kidney Cortex Extracellular Matrix-Derived Hydrogel
Published on: October 13, 2018
Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome
Rodrigo Barbosa de Souza1, Renan Barbosa Lemes1, Orestes Foresto-Neto2
1Department of Genetics and Evolutionary Biology, University of São Paulo, São Paulo, SP, Brazil.
Abstract:
Fibrillin-1 is a pivotal structural component of the kidney's glomerulus and peritubular tissue. Mutations in the fibrillin-1 gene result in Marfan syndrome (MFS), an autosomal dominant disease of the connective tissue. Although the kidney is not considered a classically affected organ in MFS, several case reports describe glomerular disease in patients. Therefore, this study aimed to characterize the kidney in the mgΔlpn-mouse model of MFS. Affected animals presented a significant reduction of glomerulus, glomerulus-capillary, and urinary space, and a significant reduction of fibrillin-1 and fibronectin in the glomerulus. Transmission electron microscopy and 3D-ultrastructure analysis revealed decreased amounts of microfibrils which also appeared fragmented in the MFS mice. Increased collagen fibers types I and III, MMP-9, and α-actin were also observed in affected animals, suggesting a tissue-remodeling process in the kidney. Video microscopy analysis showed an increase of microvessel distribution coupled with reduction of blood-flow velocity, while ultrasound flow analysis revealed significantly lower blood flow in the kidney artery and vein of the MFS mice. The structural and hemodynamic changes of the kidney indicate the presence of kidney remodeling and vascular resistance in this MFS model. Both processes are associated with hypertension which is expected to worsen the cardiovascular phenotype in MFS.
Insights
Marfan syndrome (MFS) causes kidney structural changes, including reduced glomeruli and microfibrils. This mouse model study reveals kidney remodeling and vascular resistance, potentially worsening MFS cardiovascular issues.
Area of Science:
- Nephrology
- Genetics
- Connective Tissue Diseases
Background:
- Fibrillin-1 is crucial for kidney structure.
- Mutations in fibrillin-1 cause Marfan syndrome (MFS).
- Kidney involvement in MFS is underreported but suggested by case studies.
Purpose of the Study:
- To investigate kidney structural and hemodynamic changes in a mouse model of Marfan syndrome (mgΔlpn mice).
Main Methods:
- Comparative analysis of kidney structure using microscopy (TEM, 3D-ultrastructure, video microscopy).
- Assessment of protein expression (fibrillin-1, fibronectin, collagen, MMP-9, α-actin).
- Hemodynamic evaluation via ultrasound flow analysis.
Main Results:
- MFS mice showed reduced glomeruli, urinary space, and microfibrils.
- Increased collagen, MMP-9, and α-actin indicated kidney tissue remodeling.
- Reduced blood flow and velocity in kidney vasculature were observed.
Conclusions:
- The mgΔlpn mouse model exhibits significant kidney structural and hemodynamic alterations.
- These changes suggest kidney remodeling and vascular resistance in MFS.
- These kidney issues may exacerbate the cardiovascular complications of Marfan syndrome.
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