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Plasma storage at -80 degrees C does not protect matrix metalloproteinase-9 from degradation
Didier Rouy1, Isabelle Ernens, Céline Jeanty
1Cardiovascular Research Laboratory, CRP-Santé, L-1150 Luxembourg, Luxembourg. didier.rouy@crp-sante.healthnet.lu
Abstract:
Recently, matrix metalloproteinase-9 (MMP-9) has been identified as a cardiovascular risk marker and is increasingly being determined in clinical studies. Among other matrix metalloproteinases, MMP-9 is known to be self-activable, as the cleavage of the propeptide leads to the formation of an active enzyme. In such a case the issue of storage of biological samples such as plasmas is of outstanding importance, as an enzymatic activity, although minimal, may remain at common storage temperature, i.e., -80 degrees C. Since 2000 our institute has created a plasma library from patients presenting with acute myocardial infarction. Recently, the evaluation of the MMP-9 led to the surprise of finding a dramatically low level of detectable enzyme in the oldest plasma samples. By using zymography, enzyme-linked immunosorbent assay and Western blots, we evaluated new and old samples and found that MMP-9 degrades over time. After 2 years, the detectable total MMP-9 dropped by 65%, and the asymptotic profile of the curve reached a residual 1% level after 43 months. These results were confirmed by zymography and western blotting. TIMP-1, the natural inhibitor of MMP-9 and MMP-2, remained rather stable over time. The results suggest that human plasma MMP-9 levels should be determined as soon as possible after sampling.
Insights
Matrix metalloproteinase-9 (MMP-9), a cardiovascular risk marker, degrades significantly in stored plasma over time. Detectable MMP-9 levels dropped by 65% after 2 years, emphasizing prompt analysis after sampling.
Area of Science:
- Biochemistry
- Cardiovascular Research
- Clinical Diagnostics
Background:
- Matrix metalloproteinase-9 (MMP-9) is a recognized cardiovascular risk marker.
- MMP-9 is self-activable, raising concerns about sample storage stability.
- Plasma samples from acute myocardial infarction patients have been collected since 2000.
Purpose of the Study:
- To investigate the stability of matrix metalloproteinase-9 (MMP-9) in stored human plasma.
- To determine the impact of storage duration on detectable MMP-9 levels.
- To assess the stability of TIMP-1 in relation to MMP-9 degradation.
Main Methods:
- Zymography
- Enzyme-linked immunosorbent assay (ELISA)
- Western blotting
- Analysis of plasma samples stored for varying durations.
Main Results:
- Detectable total MMP-9 levels decreased by 65% after 2 years of storage.
- Residual MMP-9 levels reached approximately 1% after 43 months.
- TIMP-1, an MMP inhibitor, demonstrated relative stability over time.
Conclusions:
- Human plasma MMP-9 degrades substantially during storage.
- Prompt determination of MMP-9 levels post-sampling is crucial for accurate clinical assessment.
- Storage conditions significantly impact the reliability of MMP-9 as a biomarker.
