The Role of Smad2 in Transforming Growth Factor ß1-Induced Hypertrophy of Ligamentum Flavum.
World Neurosurg
; 151: e128-e136, 2021 07.
Article
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| MEDLINE
| ID: mdl-33831616
ABSTRACT
BACKGROUND:
Hypertrophy of the ligamentum flavum (LF) contributes to the development of spinal stenosis. Smad proteins can mediate the fibrogenesis activity through the transforming growth factor ß1 (TGF-ß1) pathway, but which Smad protein plays a more important role in the hypertrophy process of LF is unclear.METHODS:
The LF samples were obtained from 50 patients. After the LF cells (LFCs) were cultured, small interfering ribonucleic acid (siRNA) that target human phosphorylated-Smad2, 3, or 4 (p-Smad2,3,4) genes was transfected into LFCs. Next, proteins from cells were extracted and the protein levels of Smad2, Smad3, and Smad4 were detected by Western blot. The messenger ribonucleic acid level of TGF-ß1 was measured by real-time polymerase chain reaction (PCR). Furthermore, an enzyme-linked immunosorbent assay was performed to test the impact of Smad2 downstream of the TGF-ß1 signaling pathway.RESULTS:
Degeneration of the LF was characterized by an increase in disorganized elastic fibers and fibrotic transformation by extracellular collagen deposition. The gene expression analysis of fibrotic genes in LFCs showed that knockdown of phosphorylated-Smad2 by siRNA significantly reduced the protein expression level of TGF-ß1 compared with other groups. The enzyme-linked immunosorbent assay suggested that the protein expression level of Smad2 can influence the downstream events of TGF-ß1 signaling pathway in the LFCs.CONCLUSIONS:
Our findings suggest that Smad2 plays a potential role in the pathologic development of hypertrophy of LF. We also found that Smad2 knockdown by Smad-siRNA can influence the TGF-ß1 signaling pathway through decreasing expression of TGF-ß1, tumor necrosis factor α, and nuclear factor κb.Palabras clave
Texto completo:
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Banco de datos:
MEDLINE
Asunto principal:
Ligamento Amarillo
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Proteína Smad2
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Factor de Crecimiento Transformador beta1
Límite:
Adult
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Aged
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Female
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Humans
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Male
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Middle aged
Idioma:
En
Año:
2021
Tipo del documento:
Article