Method of treating inflammtory disease associated with bone destruction
A technology for inflammatory diseases and bone destruction, applied in the field of inflammatory diseases, can solve problems such as difficult bone and joint destruction, delayed bone destruction, and weakened effect of neutralizing antibodies
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Embodiment 1
[0064] [Example 1] Raf inhibitor affects the formation of cultured osteoclasts
[0065] 1. Isolation and culture of macrophages derived from rat bone marrow
[0066] Macrophages derived from rat bone marrow were isolated and cultured with macrophage colony-stimulating factor (M-CSF). Eight Lewis rats of Charles-River grade (6-week-old, KBT Oriental Co., Ltd., Tosu, Saga) were sacrificed under anesthesia by dislocation of the neck, and the carotid artery was cut off for debleeding. The diaphysis of both femurs and tibias was removed under aseptic conditions, and the culture medium (α-modified essential medium: α-MEM (GIBCO BRL, Rockville, Maryland, USA)) was injected into the bone marrow cavity to collect bone marrow cells. Red blood cells were used 0.727% NH 4 Cl-0.017% Tris-Cl (pH7.2)-phosphate buffered saline (PBS) after washing, wash with 10% fetal bovine serum (FBS) and recombinant human M-CSF (rhM-CSF, 10ng / ml, CHEMICON International , Inc.Temecula, CA) α-MEM will b...
Embodiment 2
[0069] [Example 2] Effect of introducing sFGFR gene on AIA: extracellular blockade of FGF-2
[0070]
[0071] 1. AIA model
[0072] In order to establish the AIA model, rats were subcutaneously injected with 1 mg of dead Mycobacterium tuberculosis (Desiccated: Mycobacterium Butyricum: MBD, Difco, Detroit, MI, USA) dissolved in mineral oil (NACALAI 100 μl suspension in TESQUE, Kyoto).
[0073] 2. Protocol for Extracellular Blockade of FGF2
[0074] Direct gene transfer using a recombinant Sendai virus vector (SeV) was performed to locally express the target gene in inflammation in rats, and then the effect on arthritis was examined. Specifically, the onset of arthritis was first confirmed, and then, 14 days after the administration of the adjuvant, the AIA+sFGFR group (n=40) was administered SeV with a soluble FGF receptor gene (sFGFR, SEQ ID NO: 1) on the foot pad. (SeV-sFGFR), 10 8 pfu / foot; AIA+luciferase control group (n=28) footpad administration of SeV (SeV-lu...
Embodiment 3
[0083] [Example 3] Influence of introducing Spry2 gene on AIA: blocking FGF-2 intracellular signal
[0084]
[0085] 1. AIA model
[0086] A 100 μl suspension of 1 mg of dead Mycobacterium tuberculosis (dried Mycobacterium butyricum: MBD, Difco) dissolved in mineral oil (NACALAI TESQUE) was injected subcutaneously at the base of the tail of the rat.
[0087] 2. Protocol for Intracellular Blockade of FGF2
[0088] Direct gene transfer using a recombinant Sendai virus vector (SeV) was performed to locally express the target gene in inflammation in rats, and then the effect on arthritis was examined. Specifically, the onset of arthritis was first confirmed, and then, 14 days after the administration of the adjuvant, the AIA+Spry2 group (n=33) was administered SeV (SeV- spry2), 10 8 pfu / foot; AIA+luciferase control group (n=33) footpad administration of SeV (SeV-luciferase) with luciferase gene, 10 8 pfu / foot.
[0089] 3. Determination of hindlimb volume
[0090] H...
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