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Journal of the American Academy of Dermatology
Volume 63, n° 3
pages 483-489 (septembre 2010)
Doi : 10.1016/j.jaad.2009.09.006
Dermatopathology

The imbalanced expression of matrix metalloproteinases in nephrogenic systemic fibrosis
 

Brent C. Kelly, MD a, , Leslie Scroggins Markle, MD b, Jennifer L. Vickers, MD b, Matthew S. Petitt, DO a, Sharon S. Raimer, MD a, Catherine McNeese, MD c
a Department of Dermatology, University of Texas Medical Branch, Galveston, Texas 
b Department of Internal Medicine, University of Texas Medical Branch, Galveston, Texas 
c Reitpath Pathology, dba Brazos Valley Pathology, Round Rock, Texas 

Reprint requests: Brent C. Kelly, MD, Assistant Professor, Department of Dermatology, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555-0783.
Abstract
Background

Nephrogenic systemic fibrosis (NSF) occurs in patients with renal dysfunction and gadolinium exposure. Although little is known about the pathogenesis of this disease, increased expression of transforming growth factor-β has been recently demonstrated. Other fibrosing conditions have been shown to express an imbalance in matrix metalloproteinase (MMP) expression and their corresponding inhibitors. Myofibroblast differentiation, in which cells often express ⍺-smooth muscle actin and achieve the ability to contract, is also a hallmark of fibrosis.

Objective

We theorized that NSF may overexpress tissue inhibitor of metalloproteinase-1 (TIMP-1), while simultaneously showing decreased expression of MMP-1. As a secondary aim, we sought to evaluate the presence of smooth muscle actin in our samples.

Methods

We applied immunohistochemistry to 16 skin biopsies from 10 patients with NSF using antibodies to TIMP-1, MMP-1, MMP-2, MMP-9, and ⍺-smooth muscle actin. Samples from normal skin, scar, keloid and scleroderma were stained for comparison.

Results

TIMP-1 was strongly expressed in all NSF specimens compared to normal skin. MMP-1 expression was nearly absent in all tested samples. In all 16 NSF cases, the dermal spindle cells did not stain for ⍺-smooth muscle actin. MMP-2 and MMP-9 expression was variable but was increased compared to normal skin.

Limitations

The expression is semiquantitative and based on immunohistochemistry and unconfirmed by other techniques.

Conclusions

In NSF, TIMP-1 is strongly expressed and MMP-1 is nearly absent, characteristic of the MMP imbalances seen in other fibrosing processes. Using smooth muscle actin immunohistochemistry, there was no evidence of myofibroblast differentiation.

The full text of this article is available in PDF format.

Key words : matrix metalloproteinase, myofibroblast, nephrogenic fibrosing dermopathy, nephrogenic systemic fibrosis, smooth muscle actin, tissue inhibitor of matrix metalloproteinase, transforming growth factor

Abbreviations used : MMP, NSF, SMA, TGF-β, TIMP



 Financial support from the Department of Dermatology, University of Texas Medical Branch.
 Conflicts of interest: None.



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