Assessment of the Concentration of Transforming Growth Factor Beta 1-3 in Degenerated Intervertebral Discs of the Lumbosacral Region of the Spine
Status PubMed-not-MEDLINE Language English Country Switzerland Media electronic
Document type Journal Article
PubMed
39590357
PubMed Central
PMC11592718
DOI
10.3390/cimb46110763
PII: cimb46110763
Knihovny.cz E-resources
- Keywords
- intervertebral disc, intervertebral disc degeneration, transforming growth factor beta,
- Publication type
- Journal Article MeSH
The purpose of this study was to evaluate the feasibility of using the expression profile of transforming growth factor beta (TGF-β-1-3) to assess the progression of L/S spine degenerative disease. The study group consisted of 113 lumbosacral (L/S) intervertebral disc (IVD) degenerative disease patients from whom IVDs were collected during a microdiscectomy, whereas the control group consisted of 81 participants from whom IVDs were collected during a forensic autopsy or organ harvesting. Hematoxylin and eosin staining was performed to exclude degenerative changes in the IVDs collected from the control group. The molecular analysis consisted of reverse-transcription real-time quantitative polymerase chain reaction (RT-qPCR), an enzyme-linked immunosorbent assay (ELISA), Western blotting, and an immunohistochemical analysis (IHC). In degenerated IVDs, we noted an overexpression of all TGF-β-1-3 mRNA isoforms with the largest changes observed for TGF-β3 isoforms (fold change (FC) = 19.52 ± 2.87) and the smallest for TGF-β2 (FC = 2.26 ± 0.16). Changes in the transcriptional activity of TGF-β-1-3 were statistically significant (p < 0.05). Significantly higher concentrations of TGF-β1 (2797 ± 132 pg/mL vs. 276 ± 19 pg/mL; p < 0.05), TGF-β2 (1918 ± 176 pg/mL vs. 159 ± 17 pg/mL; p < 0.05), and TGF-β3 (2573 ± 102 pg/mL vs. 152 ± 11 pg/mL) were observed in degenerative IVDs compared with the control samples. Determining the concentration profiles of TGF-β1-3 appears to be a promising monitoring tool for the progression of degenerative disease as well as for evaluating its treatment or developing new treatment strategies with molecular targets.
Collegium Medicum WSB University 41 300 Dabrowa Gornicza Poland
Department of Forensic Medicine Jagiellonian University Medical College 31 531 Cracow Poland
Department of Neurosurgery Faculty of Medicine in Zabrze Academy of Silesia 40 555 Katowice Poland
Department of Neurosurgery Szpital sw Rafala in Cracow 30 693 Cracow Poland
Institute of Health Care National Academy of Applied Sciences in Przemyśl 37 700 Przemyśl Poland
New Medical Techniques Specjalist Hospital of St Family in Rudna Mała 36 060 Rzeszów Poland
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