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生长分化因子5(GDF5)在金纳米颗粒梯度上以浓度依赖的方式诱导T盒转录因子3(TBX3)。

GDF5 induces TBX3 in a concentration dependent manner - on a gold nanoparticle gradient.

作者信息

Andreasson L, Evenbratt H, Simonsson S

机构信息

Cline Scientific AB, Mölndal, SE-431 53, Sweden.

Institute of Biomedicine at Sahlgrenska Academy, Department of Clinical Chemistry and Transfusion Medicine, University of Gothenburg, Gothenburg, SE-413 45, Sweden.

出版信息

Heliyon. 2020 Jun 10;6(6):e04133. doi: 10.1016/j.heliyon.2020.e04133. eCollection 2020 Jun.

Abstract

Organs and tissues, such as cartilage and limbs, are formed during development through an orchestration of growth factors that function as morphogens. Examples of growth factors include growth differentiation factor 5 (GDF5) and transforming growth factors beta 1 and 3 (TGFβ-1 and TGFβ-3) which can specify creation of more than one cell type after forming a concentration gradient . Here, we studied the impact of morphogen gradients during differentiation of induced pluripotent stem cells (iPSCs) into the chondrocyte lineage. Cell budding zones, consisting of condensed cell aggregates, were observed only in gradients of GDF5. T-box transcription factor 3 (TBX3) was detected specifically in the budding zones (ranging from 500-1,500 particles/μm) of nuclei and cell vesicles. A homogenous density of GDF5 of 900 particles/μm on a surface induced budding and expression of TBX3 after five days in iPSCs. Therefore, we conclude that a gradient of GDF5, as well as the specific homogenous density of GDF5, support the induction of TBX3 in iPCSs. Moreover, differentiation of iPSCs first on GDF5 gradient or homogenous surfaces for five days and then in a three-dimensional structure for five weeks resulted in pellets that expressed TBX3.

摘要

器官和组织,如软骨和四肢,在发育过程中是通过作为形态发生素的生长因子的协同作用形成的。生长因子的例子包括生长分化因子5(GDF5)以及转化生长因子β1和β3(TGFβ-1和TGFβ-3),它们在形成浓度梯度后可指定产生不止一种细胞类型。在这里,我们研究了形态发生素梯度在诱导多能干细胞(iPSC)向软骨细胞谱系分化过程中的影响。仅在GDF5梯度中观察到由浓缩细胞聚集体组成的细胞芽区。在细胞核和细胞囊泡的芽区(范围为500 - 1500个颗粒/μm)中特异性检测到T盒转录因子3(TBX3)。在iPSC中,表面上900个颗粒/μm的均匀GDF5密度在五天后诱导了芽的形成和TBX3的表达。因此,我们得出结论,GDF5梯度以及GDF5的特定均匀密度支持iPSC中TBX3的诱导。此外,iPSC先在GDF5梯度或均匀表面上分化五天,然后在三维结构中分化五周,产生了表达TBX3的微球。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ede4/7292926/3987fedaa55e/gr1.jpg

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