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Unexpected Timely Fracture Union in Matrix Metalloproteinase 9 Deficient Mice

dc.contributor.authorYuasa, Masato
dc.contributor.authorSaito, Masanori
dc.contributor.authorMolina, Cesar
dc.contributor.authorMoore-Lotridge, Stephanie N.
dc.contributor.authorBenvenuti, Michael A.
dc.contributor.authorMignemi, Nicholas A.
dc.contributor.authorOkawa, Atsushi
dc.contributor.authorYoshii, Toshitaka
dc.contributor.authorSchwartz, Herbert S.
dc.contributor.authorNyman, Jeffry S.
dc.contributor.authorSchoenecker, Jonathan G.
dc.date.accessioned2019-02-04T19:54:44Z
dc.date.available2019-02-04T19:54:44Z
dc.date.issued2018-05-31
dc.identifier.citationYuasa M, Saito M, Molina C, Moore-Lotridge SN, Benvenuti MA, Mignemi NA, et al. (2018) Unexpected timely fracture union in matrix metalloproteinase 9 deficient mice. PLoS ONE 13(5): e0198088. https://doi.org/10.1371/journal.pone.0198088en_US
dc.identifier.issn1932-6203
dc.identifier.other10.1371/journal.pone.0198088
dc.identifier.urihttp://hdl.handle.net/1803/9374
dc.description.abstractImmediately following a fracture, a fibrin laden hematoma is formed to prevent bleeding and infection. Subsequently, the organized removal of fibrin, via the protease plasmin, is essential to permit fracture repair through angiogenesis and ossification. Yet, when plasmin activity is lost, the depletion of fibrin alone is insufficient to fully restore fracture repair, suggesting the existence of additional plasmin targets important for fracture repair. Previously, activated matrix metalloproteinase 9 (MMP-9) was demonstrated to function in fracture repair by promoting angiogenesis. Given that MMP-9 is a defined plasmin target, it was hypothesized that pro-MMP-9, following plasmin activation, promotes fracture repair. This hypothesis was tested in a fixed murine femur fracture model with serial assessment of fracture healing. Contrary to previous findings, a complete loss of MMP-9 failed to affect fracture healing and union through 28 days post injury. Therefore, these results demonstrated that MMP-9 is dispensable for timely fracture union and cartilage transition to bone in fixed femur fractures. Pro-MMP-9 is therefore not a significant target of plasmin in fracture repair and future studies assessing additional plasmin targets associated with angiogenesis are warranted.en_US
dc.language.isoen_USen_US
dc.subjectFibrin Laden Hematomaen_US
dc.subjectProtease Plasminen_US
dc.subject.lcshOrthopaedicsen_US
dc.titleUnexpected Timely Fracture Union in Matrix Metalloproteinase 9 Deficient Miceen_US
dc.typeArticleen_US
dcterms.rights© 2018 Yuasa et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_US


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