Abstract
Matrix metalloproteinases are a family of zinc-dependent proteinases which are involved in the breakdown and remodeling of extracellular matrix. As children grow and adolescents reach pubescence, their bodies undergo changes that require age-related morphogenesis of the extracellular matrix, possibly requiring unique patterns of matrix metalloproteinase (MMP) expression during periods of rapid tissue growth (i.e., childhood) or accelerated tissue remodeling and expansion (i.e., adolescence). Therefore, we have characterized age-specific and gender-specific differences in circulating concentrations of MMPs (specifically MMP-1, -2, -3, -8 and -9) in 189 serum samples obtained from healthy subjects, aged 2-18 years. MMP concentrations were measured using Fluorokine® MultiAnalyte Profiling kits and a Luminex® Bioanalyzer, as well as by commercial ELISA. Serum levels of MMP-1, -2, -3, -8, and -9 in healthy pediatric subjects represent log-normal distributions. MMP-2 was significantly negatively correlated with age (r= -0.29; p < 0.001), while MMP-3 was significantly positively correlated with age (r = 0.38; p < 0.001). Although plasma, not serum, is considered the appropriate blood sample for measurement of MMP-8 and -9, serum levels of MMP-8 and -9 were also found to be highly positively correlated with each other (r = 0.76; p < 0.01). MMP results obtained by Fluorokine® MultiAnalyte Profiling methods correlated well with conventional ELISA methods and use of this technology provided several advantages over ELISA.
Original language | English |
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Pages (from-to) | 1392-1399 |
Number of pages | 8 |
Journal | Clinical Chemistry and Laboratory Medicine |
Volume | 43 |
Issue number | 12 |
DOIs | |
State | Published - Dec 2005 |
Bibliographical note
Funding Information:This work was supported by a grant from the Arkansas Children’s Hospital Research Institute (ACHRI) Dean’s/CUMG Research Development Fund ( SG-030103-KT) and a grant from the National Institutes of Health to ACHRI (R01-DK62999-KT). The authors also acknowledge the support of the University of Arkansas for Medical Sciences’ General Clinical Research Center, grant M01 RR14288 for assistance with MMP clinical investigations.
Funding
This work was supported by a grant from the Arkansas Children’s Hospital Research Institute (ACHRI) Dean’s/CUMG Research Development Fund ( SG-030103-KT) and a grant from the National Institutes of Health to ACHRI (R01-DK62999-KT). The authors also acknowledge the support of the University of Arkansas for Medical Sciences’ General Clinical Research Center, grant M01 RR14288 for assistance with MMP clinical investigations.
Funders | Funder number |
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Arkansas for Medical Sciences’ General Clinical Research Center | M01 RR14288 |
CUMG | SG-030103-KT |
National Institutes of Health (NIH) | |
National Institute of Diabetes and Digestive and Kidney Diseases | R01DK062999 |
Arkansas Children’s Hospital Research Institute |
Keywords
- Collagenase
- Endopeptidases
- Gelatinase
- Particle-based flow cytometry
- Puberty
- Stromelysin
ASJC Scopus subject areas
- Clinical Biochemistry
- Biochemistry, medical