REN Zhou-xin, LI Jian-sheng, SHEN Jun-ling, et al. Effect of Bufei Yishen Formula on TGF-/Smad Signaling Pathway of Human Pulmonary Arterial Smooth Muscle Cells Induced by TGF- and BMP-4[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(11): 126-132.
DOI:
REN Zhou-xin, LI Jian-sheng, SHEN Jun-ling, et al. Effect of Bufei Yishen Formula on TGF-/Smad Signaling Pathway of Human Pulmonary Arterial Smooth Muscle Cells Induced by TGF- and BMP-4[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(11): 126-132. DOI: 10.13422/j.cnki.syfjx.20180937.
Effect of Bufei Yishen Formula on TGF-/Smad Signaling Pathway of Human Pulmonary Arterial Smooth Muscle Cells Induced by TGF- and BMP-4
Objective: The purpose of the study was to explore the effect of Bufei Yishen formula (BFYS) on cellular proliferation of pulmonary artery smooth muscle cells induced by transforming growth factor-β1 (TGF-β1)/bone morphogenetic protein-4 (BMP-4)
furthermore
to explore the effect of BFYS on TGF-β1/Smad signaling pathway in the cells. Method: TGF-β1/BMP-4was used to induce proliferation of human pulmonary artery smooth muscle cells. The cells were divided normal group (10% normal rat serum)
induced-proliferation group(10% normal rat serum with 7.5 μg·L-1TGF-β1 and 5 μg·L-1BMP-4)
4% BFYS serum group(6% normal rat serum with 7.5 μg·L-1TGF-β1 and 5 μg·L-1BMP-4 and 4% BFYS rat serum)
6% BFYS serum group (4% normal rat serum with 7.5 μg·L-1TGF-β1 and 5 μg·L-1BMP-4 and 6% BFYS rat serum) and 8% BFYS serum group (2% normal rat serum with 7.5 μg·L-1TGF-β1 and 5 μg·L-1BMP-4 and 8% BFYS rat serum). After 24 h induction
cell density was observed under a microscope; 5-bromo-2-deoxyuridine(BrdU) was used to detect the cellular proliferation;Western blot was used to detect the Smad 1
2
3
5 and p-Smad2/3 protein expression
and Real-time PCR was used to detect plasminogen activator inhibitor-1 (PAI-1)
connective tissue growth factor(CTGF)
dominant negative helix-loop-transcription factors-1 (ID-1)and ID-2 mRNA expression. Result: After 24 h of TGF-β1/BMP-4 treatment
the cells density was increased under micro-examination with significant increase in cellular proliferation ratio (P<0.05). BFYS inhibited TGF-β1/BMP-4-induced cellular proliferation in a dose dependent manner
with significant decrease in 8% concentration group(P<0.01). Both TGF-β1/BMP-4 and BFYS showed no significant effect on Smad1
2
3 and 5 proteins expression. However
p-Smad2/3 expression was significant increased by TGF-β1/BMP-4 induction (P<0.05) and 8% BFYS significantly reduced its expression (P<0.05). For assays of down-scream genes expression of TGF-β1/Smad pathway
TGF-β1/BMP-4 and BFYS showed no significant effect on PAI-1
ID-1and ID-2 mRNA expression. But TGF-β1/BMP-4 increased CTGF mRNA expression (P<0.01) and 8% BFYS inhibited TGF-β1/BMP-4 induced CTGF mRNA expression (P<0.05). Conclusion: BFYS reduced TGF-β1/BMP-4 induced cellular proliferation of human pulmonary arterial smooth muscle cells
and its mechanisms might be associated with inhibiting p-Smad2/3/CTGF pathway.
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