Journal: Frontiers in Bioengineering and Biotechnology
Article Title: Innate immune pathway activated mesenchymal stromal cells improve function and histologic outcomes in a rodent osteoarthritis model
doi: 10.3389/fbioe.2025.1525969
Figure Lengend Snippet: Histologic representative images of mouse knees at endterm. Toluidine blue photomicrographs from (left to right) control (needle insertion alone), MSC, TLR3-MSC, and STING-MSC treated (right) limbs. Low magnification (×4) images of whole knee joints from (left to right) control (A) , MSC (D) , TLR3-MSC (G) , and STING-MSC (J) treated joints. Higher magnification (×10) images presented for evaluation of the medial compartment of (left to right) control (B) , MSC (E) , TLR3-MSC (H) , and STING-MSC (K) treated joints. Additional higher magnification image for evaluation of the lateral compartment for control (C) , MSC (F) , TLR3-MSC (I) and STING-MSC (L) treated joints. (A,D,G,J) 4x, scale bar = 200 μm; (B,C,E,F,H,I,K,L) 10x, scale bar = 20 μm. Pink arrows represent mostly cartilagenous osteophytes. The yellow circle indicates synovitis. Red arrows highlight areas of cartilage loss to below the calcified layer. White arrows outline a roughened cartilage surface, as well as fibrillation. MSC, mesenchymal stromal cells; TLR, Toll-Like receptor; STING, Stimulator of Interferon Genes.
Article Snippet: At weeks 3 and 5, MSC were trypsinized, counted, and a portion activated with the TLR3 agonist polyinosinic-polycytidylic acid (pIC) (InVivoGen, San Diego, CA) or 2′3′cGAMP (InVivoGen, San Diego, CA) to stimulate cGAS-STING pathways (stimulation dose at 10 μg/mL at a concentration of 1 × 10 6 cells/mL in growth media for 2 h stimulation time).
Techniques: Control