Use of an anticollagenase antibody to study synovial cell interactions with particulate material

Patrick E. Greis, Helga I. Georgescu, Freddie H. Fu, Christopher H Evans

Research output: Chapter in Book/Report/Conference proceedingConference contribution


Wear particles released from synthetic anterior cruciate ligaments (ACLs) have been implicated as mediators of the effusions and synovitis that often follow ACL reconstruction. Particulate material, released as a result of abrasion and device failure, interacts with the synovial lining cells of the knee, causing inflammation, synovial hypertrophy, and cellular activation. This leads to the intraarticular release of degradative enzymes such as collagenase. By using collagenase-specific antiserum, the in vitro activation of synovial cells by small particles was observed immunofluorescently. This technique provided direct visual evidence of cellular activation as the result of the phagocytosis of particles of latex, carbon, or Dacron. Particles 23 μm and less in diameter were easily phagocytosed by the synovial cells, resulting in the production of collagenase. This method permits observation of the interactions between individual cells and particles of specific sizes, shapes, and other physical properties. It should thus prove useful in future studies of the importance of these parameters in eliciting cellular responses to particles.

Original languageEnglish (US)
Title of host publicationASTM Special Technical Publication
PublisherPubl by ASTM
Number of pages6
StatePublished - 1992
Externally publishedYes
EventSymposium on Biocompatibility of Particulate Implant Materials - San Antonio, TX, USA
Duration: Oct 31 1990Oct 31 1990


OtherSymposium on Biocompatibility of Particulate Implant Materials
CitySan Antonio, TX, USA


ASJC Scopus subject areas

  • Engineering(all)

Cite this

Greis, P. E., Georgescu, H. I., Fu, F. H., & Evans, C. H. (1992). Use of an anticollagenase antibody to study synovial cell interactions with particulate material. In ASTM Special Technical Publication (1144 ed., pp. 200-205). Publ by ASTM.