RAPID ONSET SYNOVIAL INFLAMMATION AND HYPERPLASIA INDUCED BY TRANSFORMING GROWTH FACTOR-BETA

被引:259
作者
ALLEN, JB
MANTHEY, CL
HAND, AR
OHURA, K
ELLINGSWORTH, L
WAHL, SM
机构
[1] NIDR,IMMUNOL LAB,CELLULAR IMMUNOL SECT,BLDG 30,ROOM 326,BETHESDA,MD 20892
[2] NIDR,CLIN INVEST & PATIENT CARE BRANCH,BETHESDA,MD 20892
[3] COLLAGEN CORP,CONNECT TISSUE RES LABS,PALO ALTO,CA 94303
关键词
D O I
10.1084/jem.171.1.231
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
After intraarticular injection of TGF-β1 or TGF-β2, marked swelling and erythema of the injected joints were apparent within 12-24 h. On a scale of 0 to 4, by day 3, the TGF-β-treated joints had articular indices (AI) of 3.6 ± 0.5 to 4.0 ± 0.0 compared with no response for the vehicle-injected contralateral joints. Histopathologic evaluation revealed a predominantly mononuclear phagocyte infiltrate with some neutrophils and T lymphocytes, consistent with active inflammation. The monocytic pattern of leukocyte infiltration at 2-3 d was comparable to that seen in animals with antigen-induced arthritis after 2-3 wk. Extensive synovial fibroblast hyperplasia became apparent within 48 h, likely as a result of TGF-β induction of growth factor synthesis by the accumulating monocytes. TGF-β2, a homologue of TGF-β1, was found to induce a similar level of synovitis and synovial hyperplasia consistent with its parallel monocyte and fibroblast chemotactic properties and ability to induce transcription and translation of monocyte/macrophage-derived groth factors. These data suggest that TGF-β, released by platelets and activated inflammatory cells, may play a direct role in leukocyte recruitment and activation in arthritic and other chronic inflammatory lesions.
引用
收藏
页码:231 / 247
页数:17
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