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细胞发育过程中膜流动性波动的评估揭示了时间和细胞类型特异性。

Assessment of Membrane Fluidity Fluctuations during Cellular Development Reveals Time and Cell Type Specificity.

作者信息

Noutsi Pakiza, Gratton Enrico, Chaieb Sahraoui

机构信息

Division of Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Engineering, Thuwal, KSA.

Laboratory of Fluorescence Dynamics, Biomedical Engineering Department, University of California Irvine, Irvine, California, United States of America.

出版信息

PLoS One. 2016 Jun 30;11(6):e0158313. doi: 10.1371/journal.pone.0158313. eCollection 2016.

Abstract

Cell membrane is made up of a complex structure of lipids and proteins that diffuse laterally giving rise to what we call membrane fluidity. During cellular development, such as differentiation cell membranes undergo dramatic fluidity changes induced by proteins such as ARC and Cofilin among others. In this study we used the generalized polarization (GP) property of fluorescent probe Laurdan using two-photon microscopy to determine membrane fluidity as a function of time and for various cell lines. A low GP value corresponds to a higher fluidity and a higher GP value is associated with a more rigid membrane. Four different cell lines were monitored such as hN2, NIH3T3, HEK293 and L6 cells. Membrane fluidity was measured at 12h, 72h and 92 h. Our results show significant changes in membrane fluidity among all cell types at different time points. GP values tend to increase significantly within 92 h in hN2 cells and 72 h in NIH3T3 cells and only at 92 h in HEK293 cells. L6 showed a marked decrease in membrane fluidity at 72 h and starts to increase at 92 h. As expected, NIH3T3 cells have more rigid membrane at earlier time points. On the other hand, neurons tend to have the highest membrane fluidity at early time points emphasizing its correlation with plasticity and the need for this malleability during differentiation. This study sheds light on the involvement of membrane fluidity during neuronal differentiation and development of other cell lines.

摘要

细胞膜由脂质和蛋白质的复杂结构组成,这些成分横向扩散,产生了我们所说的膜流动性。在细胞发育过程中,如细胞分化时,细胞膜会经历由ARC和Cofilin等蛋白质诱导的显著流动性变化。在本研究中,我们使用双光子显微镜,利用荧光探针Laurdan的广义极化(GP)特性来确定膜流动性随时间的变化以及不同细胞系的膜流动性情况。低GP值对应较高的流动性,而高GP值与更刚性的膜相关。我们监测了四种不同的细胞系,如hN2、NIH3T3、HEK293和L6细胞。在12小时、72小时和92小时测量膜流动性。我们的结果表明,在不同时间点,所有细胞类型的膜流动性都有显著变化。hN2细胞在92小时内、NIH3T3细胞在72小时内,GP值往往会显著增加,而HEK293细胞仅在92小时时GP值显著增加。L6细胞在72小时时膜流动性显著下降,在92小时时开始增加。正如预期的那样,NIH3T3细胞在早期时间点的膜更刚性。另一方面,神经元在早期时间点往往具有最高的膜流动性,这强调了其与可塑性的相关性以及在分化过程中这种可塑性的必要性。这项研究揭示了膜流动性在神经元分化和其他细胞系发育过程中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f72/4928918/87e34fb921a5/pone.0158313.g001.jpg

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