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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.
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http://dx.doi.org/10.3390/ani12162028 | DOI Listing |
BMC Musculoskelet Disord
August 2025
Department of Orthopedic Surgery, School of Medicine, Gaziantep Islamic Science and Technology University, Gaziantep, Turkey.
Osteogenesis Imperfecta (OI) is a connective tissue disease that is the most common genetic cause of osteoporosis and is characterized by deformities and fractures in long bones. This disease occurs due to the deficiency of Type 1 collagen. Orthopedically, it is aimed to treat and prevent deformities and fractures in the extremities.
View Article and Find Full Text PDFInt J Mol Sci
July 2025
Research Centre for Medical Genetics, Moskvorechye St., 1, 115522 Moscow, Russia.
Spondyloepimetaphyseal dysplasia type Isidor-Toutain (RPL13-SEMD) is an autosomal dominant skeletal dysplasia caused by heterozygous pathogenic variants in the gene, encoding the ribosomal protein eL13. To date, 13 pathogenic variants in have been reported, all clustering within intron 5 and exon 6, suggesting this hotspot region is critical for the function of ribosomes in skeletal tissues. Here, we present clinical and radiological characteristics of seven individuals, five children and two adults, from four unrelated families with RPL13-SEMD caused by two novel variants (c.
View Article and Find Full Text PDFJ Med Ultrasound
August 2024
Department of Fetal Medicine, NMC Royal Hospital, Abu Dhabi, United Arab Emirates.
Background: Stuve-Wiedemann syndrome (SWS) is a rare skeletal abnormality with extensive postnatal literature but limited prenatal studies. Our group had published a diagnostic algorithm to identify prenatal cases, yet, the challenge continues, especially when there is no family history of a similar condition.
Methods: We retrospectively analyzed our experience of prenatal diagnosis of SWS over an 8-year period with ethical approval.
Pestic Biochem Physiol
August 2025
College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, PR China. Electronic address:
Thiram, one of the most widely used dithiocarbamate fungicides, has turned out to be a very potent cellular metabolic homeostasis disruptor through the induction of endoplasmic reticulum (ER) stress. The present study examines the mechanistic foundation of thiram-induced tibial dyschondroplasia in birds, emphasizing ER stress and inter-organ crosstalk. According to our findings, thiram caused impairment in the function of hepatocytes, as well as inducing an inflammatory cascade of signals in the tibial growth plate and liver tissues.
View Article and Find Full Text PDFZhonghua Bing Li Xue Za Zhi
June 2025
Department of Pathology, Beijing Jishuitan Hospital, Capital Medical University, Beijing 100035, China.
To investigate the clinicopathological and genetic characteristics of malignant transformation of polyostotic fibrous dysplasia (FD) in long bone. A retrospective analysis of clinical characteristics and morphological features was conducted from 4 cases of malignant transformation of FD diagnosed at Beijing Jishuitan Hospital from January 2016 to December 2023. Hotspot mutations for GNAS gene were tested in 4 cases by Sanger sequencing, in which both FD and malignant tissues were detected in 3 cases respectively.
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