The Knee
Volume 18, Issue 4 , Pages 247-251, August 2011

Human anterior cruciate ligament fibroblasts from immature patients have a stronger in vitro response to platelet concentrates than those from mature individuals

Received 26 February 2010; received in revised form 19 May 2010; accepted 22 May 2010. published online 23 August 2010.

Abstract 

A number of recently published studies have established a substantial age dependence of the response of ACL fibroblasts to stimulation by platelet-rich plasma (PRP). Further in-depth research of this age dependence revealed negative effects on both histological and biomechanical results in a large animal model. However, while it has been postulated that this association could affect potential human applications negatively too it remains to be proven that the same effects occur in human cells. Thus it was the objective of this study to search for age dependence in human fibroblasts before further human experiments are done. Human fibroblasts were obtained from 10 immature and adolescent patients, based on a-priori power calculations, and cultured in a collagen-PRP composite. Three parameters that are pivotal for defect remodeling and wound healing—cell migration, cell proliferation, and scaffold contraction—were chosen as endpoints. Both migration and proliferation were significantly higher in immature cells, but no differences were seen in wound contraction. The former findings suggest that immature patients respond more favorably to treatment with PRP, which consequently might translate into better results in ACL tissue engineering.

Keywords: Tissue engineering, ACL, Age, Fibroblast, Repair

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0968-0160(10)00121-3

doi:10.1016/j.knee.2010.05.015

The Knee
Volume 18, Issue 4 , Pages 247-251, August 2011