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Contribution of extracellular matrix components to the stiffness of skeletal muscle contractures in patients with cerebral palsy.
Smith, Lucas R; Pichika, Rajeswari; Meza, Rachel C; Gillies, Allison R; Baliki, Marwan N; Chambers, Henry G; Lieber, Richard L.
Affiliation
  • Smith LR; Departments of Neurobiology, Physiology, and Behavior and Physical Medicine and Rehabilitation, University of California, Davis, CA, USA.
  • Pichika R; Shirley Ryan AbilityLab and Department of Physical Medicine and Rehabilitation, Northwestern University, Chicago, IL, USA.
  • Meza RC; Department of Orthopaedic Surgery, University of California San Diego, La Jolla, CA, USA.
  • Gillies AR; Department of Biology, University of California San Diego, La Jolla, CA, USA.
  • Baliki MN; Department of Orthopaedic Surgery, University of California San Diego, La Jolla, CA, USA.
  • Chambers HG; Shirley Ryan AbilityLab and Department of Physical Medicine and Rehabilitation, Northwestern University, Chicago, IL, USA.
  • Lieber RL; Department of Orthopaedics, Rady Children's Hospital, San Diego, CA, USA.
Connect Tissue Res ; 62(3): 287-298, 2021 05.
Article in En | MEDLINE | ID: mdl-31779492
Purpose: Joint contractures in children with cerebral palsy contain muscle tissue that is mechanically stiffer with higher collagen content than typically developing children. Interestingly, the correlation between collagen content and stiffness is weak. To date, no data are available on collagen types or other extracellular matrix proteins in these muscles, nor any information regarding their function. Thus, our purpose was to measure specific extracellular protein composition in cerebral palsy and typically developing human muscles along with structural aspects of extracellular matrix architecture to determine the extent to which these explain mechanical properties. Materials and Methods: Biopsies were collected from children with cerebral palsy undergoing muscle lengthening procedures and typically developing children undergoing anterior cruciate ligament reconstruction. Tissue was prepared for the determination of collagen types I, III, IV, and VI, proteoglycan, biglycan, decorin, hyaluronic acid/uronic acid and collagen crosslinking. Results: All collagen types increased in cerebral palsy along with pyridinoline crosslinks, total proteoglycan, and uronic acid. In all cases, type I or total collagen and total proteoglycan were positive predictors, while biglycan was a negative predictor of stiffness. Together these parameters accounted for a greater degree of variance within groups than across groups, demonstrating an altered relationship between extracellular matrix and stiffness with cerebral palsy. Further, stereological analysis revealed a significant increase in collagen fibrils organized in cables and an increased volume fraction of fibroblasts in CP muscle. Conclusions: These data demonstrate a novel adaptation of muscle extracellular matrix in children with cerebral palsy that includes alterations in extracellular matrix protein composition and structure related to mechanical function.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Palsy / Contracture Limits: Child / Humans Language: En Journal: Connect Tissue Res Year: 2021 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Palsy / Contracture Limits: Child / Humans Language: En Journal: Connect Tissue Res Year: 2021 Document type: Article Affiliation country: United States Country of publication: United kingdom