Biomimetic Proteoglycans Strengthen the Pericellular Matrix of Normal and Osteoarthritic Human Cartilage

In osteoarthritis (OA), degradation of cartilage pericellular matrix (PCM), the proteoglycan-rich immediate cell microniche, is a leading event of disease initiation. This study demonstrated that biomimetic proteoglycans (BPGs) can diffuse into human cartilage from both normal and osteoarthritic donors and are preferentially localized within the PCM. Applying immunofluorescence (IF)-guided AFM nanomechanical mapping, we show that this localization of BPGs increases the PCM micromodulus of both normal and OA specimens. These results illustrate the capability of BPGs to integrate with degenerative tissues and support the translational potential of BPGs for treating human OA and other diseases associated with proteoglycan degradation.

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Publication Details

Journal
ACS Biomaterials Science & Engineering
Published
2024-08-12
DOI
https://doi.org/10.1021/acsbiomaterials.4c00813
Citations
6
Primary Topic
Osteoarthritis Treatment and Mechanisms
Type
article
Field-Weighted Citation Impact
2.82

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article

Biomimetic Proteoglycans Strengthen the Pericellular Matrix of Normal and Osteoarthritic Human Cartilage

Anita Li, Elizabeth R. Kahle, Hooman Fallahi, Mary K. Mulcahey et al.
6 citations
ACS Biomaterials Science & Engineering
Osteoarthritis Treatment and Mechanisms
2.82
article

Biomimetic Proteoglycans Strengthen the Pericellular Matrix of Normal and Osteoarthritic Human Cartilage

Anita Li, Elizabeth R. Kahle, Hooman Fallahi, Mary K. Mulcahey, Michele Marcolongo, Annika R. Bergstrom, Lin Han, X. Lucas Lu, Colette E. Trouillot
article en
6 citations

Abstract

In osteoarthritis (OA), degradation of cartilage pericellular matrix (PCM), the proteoglycan-rich immediate cell microniche, is a leading event of disease initiation. This study demonstrated that biomimetic proteoglycans (BPGs) can diffuse into human cartilage from both normal and osteoarthritic donors and are preferentially localized within the PCM. Applying immunofluorescence (IF)-guided AFM nanomechanical mapping, we show that this localization of BPGs increases the PCM micromodulus of both normal and OA specimens. These results illustrate the capability of BPGs to integrate with degenerative tissues and support the translational potential of BPGs for treating human OA and other diseases associated with proteoglycan degradation.

ACS Biomaterials Science & EngineeringVol. 10(9)
Loyola University Medical Center (US), Drexel University (US), Villanova University (US), University of Delaware (US)
National Institute of Arthritis and Musculoskeletal and Skin Diseases, Division of Civil, Mechanical and Manufacturing Innovation
Zero hunger
Openalex Percentile: Top 9%
Osteoarthritis Treatment and Mechanisms
2.82
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