Physiological matrix metalloproteinase concentrations in serum during childhood and adolescence, using Luminex® Multiplex technology

Kathryn M. Thrailkill, Cindy S. Moreau, Gael Cockrell, Pippa Simpson, Rajiv Goel, Paula North, John L. Fowlkes, Robert C. Bunn

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

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 languageEnglish
Pages (from-to)1392-1399
Number of pages8
JournalClinical Chemistry and Laboratory Medicine
Volume43
Issue number12
DOIs
StatePublished - 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.

FundersFunder number
Arkansas for Medical Sciences’ General Clinical Research CenterM01 RR14288
CUMGSG-030103-KT
National Institutes of Health (NIH)
National Institute of Diabetes and Digestive and Kidney DiseasesR01DK062999
Arkansas Children’s Hospital Research Institute

    Keywords

    • Collagenase
    • Endopeptidases
    • Gelatinase
    • Particle-based flow cytometry
    • Puberty
    • Stromelysin

    ASJC Scopus subject areas

    • Clinical Biochemistry
    • Biochemistry, medical

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