The photosensitive endoplasmic reticulum-chloroplast contact site.

IF 1.5 4区 工程技术 Q3 MICROSCOPY Journal of microscopy Pub Date : 2024-12-04 DOI:10.1111/jmi.13377
Sara N Maynard, Lawrence R Griffing
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Abstract

The endoplasmic reticulum (ER) forms contact sites with the chloroplast. Exposing contact sites that contain both the chloroplast and the ER to localised high-fluence, wavelength specific, 405 nm violet light, hereinafter referred to as photostimulation, induces multiple, potentially interacting intra- and intercellular responses. The responses vary depending on the tissue type of the cell and the chloroplast. Photostimulating the ER-chloroplast contact sites in growing epidermal cells of the hypocotyl of Arabidopsis thaliana, produces a wave of cytoplasmic ionic calcium that traverses the cell, spreading radially to other cells around the circumference of the hypocotyl. A transient ER stress accompanies the calcium wave. These responses occur in older epidermal cells (5-8 days post-germination) with nonmotile chloroplasts tethered to the ER and the cell cortex but do not occur with motile or dividing chloroplasts. Dividing chloroplasts show a markedly different association with the ER, which forms a ring around the fission plane, similar to that of dividing mitochondria. Inhibition of calcium channels with lanthanum has no effect. Photostimulation of only the ER results in no ER stress and a calcium wave with a different spatiotemporal signature: delayed release and lower magnitude, with no accompanying ER stress response. Likewise, photostimulation of the chloroplast only, without the ER, produces no calcium wave or ER stress. General chloroplast photobleaching or restructuring caused by photostimulation is not the cause of this response; photostimulation with 488 nm of the same intensity and power as 405 nm photostimulation produces no change in cytosolic calcium levels. The pH of the ER decreases, indicating the involvement of ER ion transporters in the response. A wave of increased reactive oxygen species (ROS) in mitochondria and nuclei accompanies photostimulation. Together, these data support a model by which tethered ER-chloroplast contact sites constitute a unique subcellular photosensitive region and are part of an ER-mediated signalling network. Lay Abstract: The endoplasmic reticulum (ER) forms contact sites with the chloroplast. Shining violet (405 nm) light on the chloroplast with its associated ER produces a calcium wave through the cell that is communicated to other cells. This is correlated with a wave of transient denaturation of the luminal proteins of the ER (ER stress) and increased reactive oxygen species (ROS) in mitochondria. The wavelength dependence and precise cellular location of the light stimulation implies a novel way for plants to sense light. The movement of the response through the cell is consistent with the mediation of the response by a subcellular network, such as that formed by the ER.

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光敏内质网-叶绿体接触部位。
内质网(ER)与叶绿体形成接触位点。将含有叶绿体和内质网的接触部位暴露于局部高通量、波长特定的405 nm紫光下(以下简称光刺激),可诱导多种可能相互作用的细胞内和细胞间反应。这种反应取决于细胞和叶绿体的组织类型。光刺激拟南芥生长中的下胚轴表皮细胞的内质-叶绿体接触点,产生细胞质离子钙波,该波穿过细胞,沿下胚轴圆周向其他细胞扩散。瞬态内质网应力伴随钙波。这些反应发生在较老的表皮细胞中(萌发后5-8天),非运动叶绿体与内质网和细胞皮层相连,但不发生在运动或分裂的叶绿体中。分裂的叶绿体与内质网表现出明显不同的联系,内质网在分裂平面周围形成一个环,类似于分裂的线粒体。镧对钙通道的抑制没有效果。仅对内质网进行光刺激不会产生内质网应激,并产生具有不同时空特征的钙波:释放延迟且强度较低,不伴有内质网应激反应。同样,光刺激叶绿体而不产生内质网,也不会产生钙波或内质网胁迫。一般由光刺激引起的叶绿体光漂白或重组不是这种反应的原因;488 nm光刺激与405 nm光刺激强度和功率相同,对胞质钙水平没有影响。内质网的pH值降低,表明内质网离子转运体参与了反应。随着光刺激,线粒体和细胞核中的活性氧(ROS)增加。总之,这些数据支持了一个模型,通过该模型,系住的内质网叶绿体接触位点构成了一个独特的亚细胞光敏区域,并且是内质网介导的信号网络的一部分。摘要:内质网(ER)与叶绿体形成接触位点。将紫光(405纳米)照射到叶绿体及其相关的内质网上,会产生钙波,通过细胞传递给其他细胞。这与内质网内腔蛋白的短暂变性(内质网应激)和线粒体中活性氧(ROS)的增加有关。光刺激的波长依赖性和精确的细胞定位为植物感知光提供了一种新的途径。反应通过细胞的运动与亚细胞网络(如内质网)对反应的调解是一致的。
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来源期刊
Journal of microscopy
Journal of microscopy 工程技术-显微镜技术
CiteScore
4.30
自引率
5.00%
发文量
83
审稿时长
1 months
期刊介绍: The Journal of Microscopy is the oldest journal dedicated to the science of microscopy and the only peer-reviewed publication of the Royal Microscopical Society. It publishes papers that report on the very latest developments in microscopy such as advances in microscopy techniques or novel areas of application. The Journal does not seek to publish routine applications of microscopy or specimen preparation even though the submission may otherwise have a high scientific merit. The scope covers research in the physical and biological sciences and covers imaging methods using light, electrons, X-rays and other radiations as well as atomic force and near field techniques. Interdisciplinary research is welcome. Papers pertaining to microscopy are also welcomed on optical theory, spectroscopy, novel specimen preparation and manipulation methods and image recording, processing and analysis including dynamic analysis of living specimens. Publication types include full papers, hot topic fast tracked communications and review articles. Authors considering submitting a review article should contact the editorial office first.
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