The intra-articular injection of RANKL-binding peptides inhibits cartilage degeneration in a murine model of osteoarthritis

Autor: Yukihiko Tamura, Ramachandran Murali, Kazuhiro Aoki, Yasuhiko Tabata, Yuki Yoshinari, Md. Zahirul Haque Bhuyan, Eri Sone, Chizuko Maeda, Mariko Takahashi, Yoshihiro Waki
Rok vydání: 2017
Předmět:
0301 basic medicine
musculoskeletal diseases
Cartilage
Articular

Male
Peptide
Osteoarthritis
Bone and Bones
Cell Line
Injections
Intra-Articular

03 medical and health sciences
0302 clinical medicine
Cartilage repair
Chondrocytes
Mesenchymal cell proliferation
medicine
Animals
Humans
Receptor
Cell Proliferation
030203 arthritis & rheumatology
Pharmacology
chemistry.chemical_classification
Osteoblasts
biology
Chemistry
Cartilage
Mesenchymal stem cell
lcsh:RM1-950
RANK Ligand
Osteoblast
Cell Differentiation
Mesenchymal Stem Cells
medicine.disease
Cell biology
Iodoacetic Acid
Mice
Inbred C57BL

030104 developmental biology
medicine.anatomical_structure
lcsh:Therapeutics. Pharmacology
RANKL
Immunology
biology.protein
Molecular Medicine
Monosodium iodoacetate (MIA)
RANKL-binding peptide
Oligopeptides
Zdroj: Journal of Pharmacological Sciences, Vol 134, Iss 2, Pp 124-130 (2017)
ISSN: 1347-8648
Popis: We recently found that the receptor activator of NF-κB ligand (RANKL)-binding peptide, OP3-4 stimulated the differentiation of both chondrocytes and osteoblasts. OP3-4 is also shown to inhibit cartilage degeneration. To clarify whether the peptide can inhibit cartilage degeneration without stimulating bone formation, we first performed a proliferation assay using C3H10T1/2 (the murine mesenchymal stem cell line), which is the common origin of both chondrocytes and osteoblasts. The RANKL-binding peptides, OP3-4 and W9, promoted cellular proliferation at 24 and 48 h, respectively. Next, we injected both peptides into the intra-articular space of the knee joints of mice with monosodium-iodoacetate (MIA)-induced osteoarthritis to clarify the effects of the peptides on cartilage tissue. Twenty-five nine-week-old male C57BL/6J mice received injections of vehicle, or the same molar amount of W9, OP3-4, or a control peptide (which could not stimulate osteoblast differentiation) on days 7, 14, and 21 after the injection of MIA. The mice were sacrificed on day 28. The histomorphometric analyses revealed that both peptides inhibited the degeneration of cartilage without enhancing bone formation activity. Our data suggest that the stimulation of mesenchymal cell proliferation by the RANKL-binding peptides might lead to the inhibition of cartilage degeneration.
Databáze: OpenAIRE