针对增强炎症的细胞群可以减轻骨关节炎相关的疼痛
Akshay Pandey1, Mamta Singla1, Ana Geller1
1Department of Orthopaedic Surgery, Stanford School of Medicine, 240, Pasteur Drive, Biomedical Innovations Bldg, Stanford, CA, 94034, USA.
Arthritis research & therapy
|February 17, 2024
概括
骨关节炎 (OA) 中的炎症增强细胞通过分泌特定的细胞因子,促进疼痛. 抑制这些细胞中的Jnk信号通路减少了小鼠的OA相关疼痛,提供了潜在的治疗标.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
- 疼痛研究 疼痛研究
背景情况:
- 骨关节炎 (OA) 疼痛机制尚未完全理解.
- 表达IL1R1和TNF-R2的炎症增强 (Inf-A) 细胞在人类OA软骨中发现.
- 这些Inf-A细胞表现出活跃的Jnk信号.
研究的目的:
- 为了研究软骨寄存IL1R1+TNF-R2+ Inf-A细胞在OA中的作用.
- 为了确定调节Inf-A细胞中的Jnk信号对OA的影响.
- 评估对关节结构和与疼痛相关的步态参数的影响.
主要方法:
- 在老年小鼠和OA诱导的小鼠中研究了Inf-A细胞扩张.
- 在小鼠和人类OA扩散体中,Jnk信号被抑制.
- 分析了对关节结构,步态和炎症性细胞因子的影响.
主要成果:
- 抑制Jnk可以减少炎症性细胞因子CCL2和CCL7,但不能改善关节结构.
- 在小鼠中,Jnk抑制显著改善了步态参数,表明减少了OA疼痛.
- 治疗JNK抑制剂并没有改善人类的OA软骨.
结论:
- 关节软骨中居住的Inf-A细胞通过CCL2和CCL7分泌物,有助于OA疼痛.
- 针对Inf-A细胞中的Jnk信号是一种潜在的OA疼痛管理策略.
- 需要进一步的研究来将这些发现转化为人类OA治疗.
相关概念视频
T Cell Types and Functions
1.0K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
1.0K
Analgesia and Pain Management
623
Pain is critical to various clinical pathologies, provoking an urgent need for effective management. Pain, whether acute or chronic, is a complex neurochemical process. Its alleviation depends on the type, with nonopioid analgesics effective for mild to moderate pain, such as musculoskeletal or inflammatory pain, while neuropathic pain responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors. For severe acute or chronic pain, opioids may be...
623
Inflammatory Response
2.0K
An inflammatory response is a localized, nonspecific immune reaction that occurs when a tissue is injured. It is characterized by redness, swelling, heat, and pain, which are commonly called the cardinal signs and symptoms of inflammation. Inflammation can sometimes result in a loss of function.
Inflammation can be triggered by various stimuli, such as impact, abrasion, chemical irritation, infections, and extreme hot or cold temperatures. These can damage cells and connective tissue fibers,...
Inflammation can be triggered by various stimuli, such as impact, abrasion, chemical irritation, infections, and extreme hot or cold temperatures. These can damage cells and connective tissue fibers,...
2.0K
Nociception
27.9K
Nociception—the ability to feel pain—is essential for an organism’s survival and overall well-being. Noxious stimuli such as piercing pain from a sharp object, heat from an open flame, or contact with corrosive chemicals are first detected by sensory receptors, called nociceptors, located on nerve endings. Nociceptors express ion channels that convert noxious stimuli into electrical signals. When these signals reach the brain via sensory neurons, they are perceived as pain.
27.9K
The JAK-STAT Signaling Pathway
8.9K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
8.9K


