SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Flanagan K.)
 

Search: WFRF:(Flanagan K.) > (1997-1999) > Aggrecan degradatio...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist
  • Lark, Michael W.SmithKline Beecham Pharmaceuticals (author)

Aggrecan degradation in human cartilage : Evidence for both matrix metalloproteinase and aggrecanase activity in normal, osteoarthritic, and rheumatoid joints

  • Article/chapterEnglish1997

Publisher, publication year, extent ...

  • 1997

Numbers

  • LIBRIS-ID:oai:lup.lub.lu.se:c4b026f1-160c-4088-af3c-b5ba567e67af
  • https://lup.lub.lu.se/record/c4b026f1-160c-4088-af3c-b5ba567e67afURI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:art swepub-publicationtype
  • Subject category:ref swepub-contenttype

Notes

  • To examine the activity of matrix metalloproteinases (MMPs) and aggrecanase in control and diseased human articular cartilage, metabolic fragments of aggrecan were detected with monospecific antipeptide antibodies. The distribution and quantity of MMP-generated aggrecan G1 fragments terminating in VDIPEN341 were compared with the distribution of aggrecanase-generated G1 fragments terminating in NITEGE373. Both types of G1 fragments were isolated from osteoarthritic cartilage. The sizes were consistent with a single enzymatic cleavage in the interglobular domain region, with no further proteolytic processing of these fragments. Both neoepitopes were also detected by immunohistochemistry in articular cartilage from patients undergoing joint replacement for osteoarthritis (OA), rheumatoid arthritis (RA), and in cartilage from adults with no known joint disease. In control specimens, the staining intensity for both G1 fragments increased with age, with little staining in cartilage from 22-wk-old fetal samples. There was also an increase with age in the extracted amount of MMP- generated neoepitope in relation to both aggrecan and collagen content, confirming the immunohistochemical results. After the age of 20-30 yr this relationship remained at a steady state. The staining for the MMP-generated epitope was most marked in control cartilage exhibiting histological signs of damage, whereas intense staining for the aggrecanase-generated fragment was often noted in adult cartilage lacking overt histological damage. Intense staining for both neoepitopes appeared in the more severely fibrillated, superficial region of the tissue. Intense immunostaining for both VDIPEN- and NITEGE-neoepitopes was also detected in joint cartilage from patients with OA or RA. Cartilage in these specimens was significantly more degraded and high levels of staining for both epitopes was always seen in areas with extensive cartilage damage. The levels of extracted VDIPEN neoepitope relative to collagen or aggrecan in both OA and RA samples were similar to those seen in age-matched control specimens. Immunostaining for both types of aggrecan fragments was seen surrounding the cells but also further removed in the interterritorial matrix. In some regions of the tissue, both neoepitopes were found while in others only one was detected. Thus, generation and/or turnover of these specific catabolic aggrecan fragments is not necessarily coordinated. Our results are consistent with the presence in both normal and arthritic joint cartilage of proteolytic activity against aggrecan based on both classical MMPs and 'aggrecanase'.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Bayne, Ellen K.University of Cincinnati (author)
  • Flanagan, JamieUniversity of Cincinnati (author)
  • Harper, Coral F.University of Cincinnati (author)
  • Hoerrner, Lori A.University of Cincinnati (author)
  • Hutchinson, Nancy I.University of Cincinnati (author)
  • Singer, Irwin I.University of Cincinnati (author)
  • Donatelli, Susan A.University of Cincinnati (author)
  • Weidner, Jeffrey R.University of Cincinnati (author)
  • Williams, Hollis R.University of Cincinnati (author)
  • Mumford, Richard A.University of Cincinnati (author)
  • Lohmander, L. StefanLund University,Lunds universitet,Ortopedi, Lund,Sektion III,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Orthopaedics (Lund),Section III,Department of Clinical Sciences, Lund,Faculty of Medicine,Skåne University Hospital(Swepub:lu)ort-slo (author)
  • SmithKline Beecham PharmaceuticalsUniversity of Cincinnati (creator_code:org_t)

Related titles

  • In:Journal of Clinical Investigation100:1, s. 93-1060021-9738

Internet link

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view