Regulatory Role of Apoptotic and Inflammasome Related Proteins and Their Possible Functional Aspect in Thiram Associated Tibial Dyschondroplasia of Poultry.
Muhammad Fakhar-E-Alam KulyarWangyuan YaoQuan MoYanmei DingYan ZhangJindong GaoKewei LiHuachun PanShah NawazMuhammad ShahzadKhalid MehmoodMudassar IqbalMuhammad AkhtarZeeshan Ahmad BhuttaMuhammad WaqasJia-Kui LiDe-Sheng QiPublished in: Animals : an open access journal from MDPI (2022)
Tibial dyschondroplasia debilities apoptotic and inflammasomal conditions that can further destroy chondrocytes. Inflammasomes are specialized protein complexes that process pro-inflammatory cytokines, e.g., interleukin-1β (IL-1β) and IL-18. Moreover, there is mounting evidence that many of the signaling molecules that govern programmed cell death also affect inflammasome activation in a cell-intrinsic way. During the last decade, apoptotic functions have been described for signaling molecules involving inflammatory responses and cell death pathways. Considering these exceptional developments in the knowledge of processes, this review gives a glimpse of the significance of these two pathways and their connected proteins in tibial dyschondroplasia. The current review deeply elaborates on the elevated level of signaling mediators of mitochondrial-mediated apoptosis and the inflammasome. Although investigating these pathways' mechanisms has made significant progress, this review identifies areas where more study is especially required. It might lead to developing innovative therapeutics for tibial dyschondroplasia and other associated bone disorders, e.g., osteoporosis and osteoarthritis, where apoptosis and inflammasome are the significant pathways.
Keyphrases
- cell death
- total knee arthroplasty
- cell cycle arrest
- anti inflammatory
- oxidative stress
- anterior cruciate ligament reconstruction
- bone mineral density
- healthcare
- postmenopausal women
- rheumatoid arthritis
- cell therapy
- single cell
- small molecule
- transcription factor
- stem cells
- endoplasmic reticulum stress
- signaling pathway
- dna methylation
- binding protein