RT Journal Article
SR Electronic
T1 Collagen-binding integrin α11β1 contributes to joint destruction in arthritic hTNFtg mice
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2022.01.14.476301
DO 10.1101/2022.01.14.476301
A1 Adrian Deichsel
A1 Anna De Giuseppe
A1 Isabel Zeinert
A1 Kerstin Rauwolf
A1 Ning Lu
A1 Denise Beckmann
A1 Annika Krause
A1 Beate Eckes
A1 Uwe Hansen
A1 Daniel Kronenberg
A1 Donald Gullberg
A1 Thomas Pap
A1 Adelheid Korb-Pap
YR 2022
UL http://biorxiv.org/content/early/2022/01/14/2022.01.14.476301.abstract
AB Background In rheumatoid arthritis (RA), fibroblast like synoviocytes (FLS) undergo a “tumor-like” transformation, wherein they develop an aggressive phenotype that is characterized by increased adhesion to components of cartilage extracellular matrix (ECM) and that contributes extensively to joint destruction. The collagen binding integrin α11β1 was previously shown to be involved in similar processes in cancer-associated fibroblasts mediating tumorigenicity and metastasis in certain tumors. Therefore, this study aimed to study the role of integrin α11β1 in RA and to characterize the effects of α11β1 deficiency on the disease course and severity in arthritic hTNFtg mice.Methods The expression levels of integrin α11β1 were analyzed by immunohistochemistry, immunofluorescence, and western blot analysis in synovial samples and FLS of patients with RA and osteoarthritis (OA) as well as in samples from wild type (wt) and arthritic hTNFtg mice. Furthermore, the subcellular expression of integrin α11β1 was investigated in co-culture experiments with cartilage explants and analyzed by transmission electron microscopy. To investigate the effects of integrin α11β1 deficiency, itga11-/- mice were interbred with hTNFtg mice and disease severity was assessed by clinical scoring of grip strength and paw swelling over the disease course. Hind paws of 12-weeks-old mice of all genotypes were analyzed by µCT imaging followed by stainings of paraffin-embedded tissue sections with Toluidine-blue and tartrate-resistant acid phosphatase (TRAP) to evaluate established parameters of joint destruction such as inflammation area, cartilage destaining, FLS attachment to the cartilage surface, and bone damage.Results Expression levels of integrin α11β1 were clearly elevated in synovial tissues and FLS from RA patients and hTNFtg mice, compared to the controls derived from OA patients and wt mice. Interestingly, this expression was shown to be particularly localized in focal adhesions of the FLS. As revealed by transmission electron microscopy, integrin α11β1 expression was particularly evident in areas of direct cellular contact with the ECM of cartilage. Evaluations of clinical scorings and histomorphological analyses demonstrated that itga11-/-hTNFtg displayed alleviated clinical symptoms, higher bone volume, less cartilage destruction and reduced FLS attachment to the cartilage in comparison to hTNFtg mice.Conclusions The collagen-binding integrin α11β1 is upregulated in the context of RA and its deficiency in mice with an inflammatory hTNFtg background leads to a significant reduction in the arthritic phenotype which makes integrin α11β1 an interesting target for therapeutical intervention.Competing Interest StatementThe authors have declared no competing interest.