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至少有三种转运蛋白可能介导了苏氨酸摄取,这是维持小鼠胚胎干细胞增殖所必需的。

At Least Three Transporters Likely Mediate Threonine Uptake Needed for Mouse Embryonic Stem Cell Proliferation.

机构信息

Department of Biochemistry, Midwestern University College of Health Science Downers Grove, IL, USA.

出版信息

Front Cell Dev Biol. 2016 Mar 15;4:17. doi: 10.3389/fcell.2016.00017. eCollection 2016.

Abstract

Stem cells are at the forefront of current regenerative and biomedical research. Thus, there exists an imperative and urgent need to understand the mechanisms that drive stem cell function in order to exploit their use as a therapeutic tool. Amino acids are potent inducers of signaling cascades that drive stem cell proliferation and differentiation. With a focus on mouse embryonic stem (mES) cells, Threonine (Thr) is the only amino acid required in culture media for mES cell proliferation. Current research associates this need for Thr with threonine dehydrogenase (TDH), which catabolizes Thr to glycine and acetyl-CoA in mES cells. This theory depends, in part, on the ability of 3- hydroxynorvaline (3-HNV) to inhibit both TDH and mES cell proliferation. However, the concentration of 3-HNV needed to inhibit mES cell proliferation is more than an order of magnitude less than its apparent Ki for TDH inhibition. Additionally, 3-HNV inhibits human embryonic stem (hES) cell proliferation, but hES cells do not express a functional tdh gene. Such findings indicate another mechanism for Thr stimulated mES and hES cell proliferation. Since amino acid transporters may be inducers of signaling cascades, we characterized the Thr transport systems in mES cells. We found that there is a Na(+)-dependent and a Na(+)-independent component of substrate-saturable transport, with the Na(+)-dependent component predominating. We also found that of 20 amino acids tested, the amino acids that were the strongest inhibitors of the Na(+)-dependent component of radiolabeled Thr transport were Ser, Cys, 4-OH-Pro, Asn, Met, and non-radiolabeled Thr itself. Such findings are consistent with characteristics of the ASC transport system, suggesting that this ASC system is responsible for the majority of Thr transport in mES cells. We confirmed expression of mRNA encoding the ASC system transporters, ASCT1 and ASCT2, in mES cells using RT-PCR. In conclusion, mES cells likely express at least three transporters of Thr; at least two Na(+)-dependent transporters and one Na(+)-independent one.

摘要

干细胞是当前再生医学和生物医学研究的前沿领域。因此,迫切需要了解驱动干细胞功能的机制,以便将其用作治疗工具。氨基酸是驱动干细胞增殖和分化的信号级联反应的有效诱导剂。以小鼠胚胎干细胞 (mES) 细胞为例,苏氨酸 (Thr) 是 mES 细胞培养中唯一需要的氨基酸。目前的研究将这种对 Thr 的需求与 threonine dehydrogenase (TDH) 联系起来,TDH 在 mES 细胞中可将 Thr 分解代谢为甘氨酸和乙酰辅酶 A。该理论部分取决于 3-羟基正缬氨酸 (3-HNV) 抑制 TDH 和 mES 细胞增殖的能力。然而,抑制 mES 细胞增殖所需的 3-HNV 浓度比其对 TDH 抑制的表观 Ki 低一个数量级以上。此外,3-HNV 抑制人胚胎干细胞 (hES) 细胞的增殖,但 hES 细胞不表达功能性 tdh 基因。这些发现表明了 Thr 刺激 mES 和 hES 细胞增殖的另一种机制。由于氨基酸转运体可能是信号级联反应的诱导剂,我们对 mES 细胞中的 Thr 转运系统进行了表征。我们发现存在依赖 Na+和非依赖 Na+的底物饱和转运的组成部分,其中依赖 Na+的组成部分占主导地位。我们还发现,在所测试的 20 种氨基酸中,最强的依赖 Na+的放射性标记 Thr 转运的抑制剂是 Ser、Cys、4-OH-Pro、Asn、Met 和非放射性标记 Thr 本身。这些发现与 ASC 转运系统的特征一致,表明该 ASC 系统负责 mES 细胞中 Thr 转运的大部分。我们使用 RT-PCR 确认了 mES 细胞中编码 ASC 系统转运体 ASCT1 和 ASCT2 的 mRNA 的表达。总之,mES 细胞可能至少表达三种 Thr 转运体;至少两种依赖 Na+的转运体和一种非依赖 Na+的转运体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e864/4791362/dbe9d35cbc00/fcell-04-00017-g0001.jpg

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