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切应力对挪威云杉体细胞胚胎早期形态和生长的影响。

Effects from shear stress on morphology and growth of early stages of Norway spruce somatic embryos.

机构信息

Georgia Institute of Technology, Atlanta, 30332, USA.

出版信息

Biotechnol Bioeng. 2010 Feb 15;105(3):588-99. doi: 10.1002/bit.22554.

Abstract

The shear stress effect on directional expansion of pro embryogenic masses (PEMs) and suspensor cell development of somatic embryos of Norway spruce (Picea abies) at the proliferation stage was studied by a direct and quantitative image analysis system. The experimental system allowed for detailed observations of the effect of hydrodynamic shear stress in rotating and deforming liquid cultures of proliferating Norway spruce somatic embryos. Briefly, somatic embryos at an early development stage comprised only of clusters of meristematic cells without suspensor cells were fixed on an alginate film. The alginate film was affixed on the bottom of a flow cell and the somatic embryos were subjected to laminar flow through the chamber of the flow cell. Magnified images of the cell clusters were collected every 24 h. The image data was processed based on a normalized cross-correlation method, capable of measuring morphological and size features of individual cell clusters in both temporal and spatial domains. No suspensor cells developed in the cell clusters under shear stress of 140 s(-1) for the duration of the experiments. Cell clusters in the control cultured in stationary liquid conditions developed suspensor cells after 5-9 days in culture. Furthermore, the radial growth of meristematic cell clusters was inhibited by shear rates of 86 and 140 s(-1), corresponding to shear stress of 0.086 and 0.14 N/m(2), compared to growth under stationary conditions. The shear rate showed a significant negative correlation to growth rate. Control group showed no preference for direction during growth under static conditions.

摘要

采用直接和定量的图像分析系统研究了切应力对挪威云杉(Picea abies)增殖阶段胚性愈伤组织(PEMs)的定向扩展和体细胞胚悬浮细胞发育的影响。该实验系统允许详细观察旋转和变形液体培养中挪威云杉体细胞胚的流体切应力的影响。简要地说,处于早期发育阶段的体细胞胚仅由没有悬浮细胞的分生细胞簇组成,将其固定在藻酸盐膜上。藻酸盐膜贴在流动池的底部,体细胞胚通过流动池的腔室经受层流。每隔 24 小时收集细胞簇的放大图像。根据归一化互相关方法处理图像数据,该方法能够在时空域中测量单个细胞簇的形态和大小特征。在实验持续期间,在 140 s(-1)的切应力下,细胞簇中没有发育出悬浮细胞。在静止液体条件下培养的对照细胞簇在培养 5-9 天后发育出悬浮细胞。此外,与静止条件下的生长相比,在 86 和 140 s(-1)的剪切速率下,分生细胞簇的径向生长受到抑制,这对应于 0.086 和 0.14 N/m(2)的剪切应力。剪切速率与生长速率呈显著负相关。在静态条件下生长的对照组没有表现出对方向的偏好。

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