Inhibition of BMP-mediated SMAD pathway supports the pluripotency of pig embryonic stem cells in the absence of feeder cells

被引:0
作者
Choi, Kwang-Hwan [1 ,2 ,3 ]
Lee, Dong-Kyung
Jeong, Jinsol
Ahn, Yelim [2 ,3 ]
Go, Du -Min
Kim, Dae-Yong [4 ]
Lee, Chang-Kyu [2 ,3 ,5 ]
机构
[1] Space F Corp, Res & Dev Ctr, Hwaseong 18471, Gyeonggi Do, South Korea
[2] Seoul Natl Univ, Anim Biotechnol Major, Dept Agr Biotechnol, Seoul 08826, South Korea
[3] Seoul Natl Univ, Res Inst Agr & Life Sci, Seoul 08826, South Korea
[4] Seoul Natl Univ, Coll Vet Med, Dept Vet Pathol, Seoul 08826, South Korea
[5] Seoul Natl Univ, Inst Green Bio Sci & Technol, Pyeong Chang 25354, South Korea
基金
新加坡国家研究基金会;
关键词
BMP signaling pathway; Chemokines; Feeder -free culture; LDN-193189; Pig embryonic stem cells; MAINTAINS PLURIPOTENCY; CONDITIONED MEDIUM; NUCLEAR TRANSFER; CULTURE-SYSTEM; DIFFERENTIATION; MOUSE; DERIVATION; CHEMOKINE; GROWTH; PROPAGATION;
D O I
10.1016/j.theriogenology.2024.05.027
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Here, we examined the effects of the BMP signaling pathway inhibitor LDN-193189 on the pluripotency of porcine embryonic stem cells (ESCs) in the absence of feeder cells using molecular and transcriptomic techniques. Additionally, the effects of some extracellular matrix components on porcine ESC pluripotency were evaluated to develop an optimized and sustainable feeder-free culture system for porcine ESCs. Feeder cells were found to play an important role in supporting the pluripotency of porcine ESCs by blocking trophoblast and mesodermal differentiation through the inhibition of the BMP pathway. Additionally, treatment with LDN193189, an inhibitor of the BMP pathway, maintained the pluripotency and homogeneity of porcine ESCs for an extended period in the absence of feeder cells by stimulating the secretion of chemokines and suppressing differentiation, based on transcriptome analysis. Conclusively, these results suggest that LDN-193189 could be a suitable replacement for feeder cells in the maintenance of porcine ESC pluripotency during culture. Additionally, these findings contribute to the understanding of pluripotency gene networks and comparative embryogenesis.
引用
收藏
页码:67 / 80
页数:14
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