共查询到19条相似文献,搜索用时 125 毫秒
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细胞程序死亡是多细胞生物体在内源发育信号或外源环境信号作用下在特定时间和空间发生的细胞死亡过程, 在植物的生长发育过程中起着重要作用。该文介绍了植物细胞程序死亡类型的几种划分方法、植物发育性细胞程序死亡研究常用的实验体系, 并着重概述有关植物发育性细胞程序死亡发生机制的研究进展。 相似文献
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第二讲 高等植物酶合成的调节——基因表达 总被引:1,自引:0,他引:1
一、序言植物体许多重要的生理过程如发育、分化,对环境条件的反应等无不与基因的活动相联系。高等植物细胞全能性的发现,证实了植物细胞中含有全套的遗传信息,至于细胞中特异的遗传信息的表达,则是受内部和 相似文献
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被子植物有性生殖过程中的细胞程序死亡 总被引:14,自引:2,他引:12
田惠桥 《植物生理与分子生物学学报》2002,28(3):161-168
细胞程序死亡是植物发育过程中的一种普遍现象。早就认识到高等植物生殖器官中一些细胞的死亡对植物有性生殖具有重要作用。这些细胞的死亡过程与动物组织中的细胞程序死亡基本相同。但植物体内诱导生殖细胞程序死亡的信号及其传导系统则显示出其特点 ,有些还表现出雌、雄性细胞的相互作用。探索植物生殖过程中的细胞程序死亡现象将有利于澄清植物生殖过程中的一些机理问题 ,使过去的细胞学研究结果深入到分子水平进行探讨 相似文献
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植物修复因投资成本低、环境扰动少、二次污染易控制、美化环境等优点成为重金属污染土壤修复重要的治理技术。植物内源细胞分裂素调控植物生理活动,外源细胞分裂素对植物生理生态特征产生显著影响,且在植物修复中逐渐受到研究人员的关注。细胞分裂素能够调控植物根茎发育、叶片衰老、激素传递等过程,同时在重金属胁迫下也参与蒸腾、光合、抗性、解毒等系统的运转。以细胞分裂素对植物生理活动的调控作用研究为基础,阐述了细胞分裂素在植物修复中的作用机制。主要包括:增强光合作用,延缓叶片衰老,提升植物抗性能力;调控根茎叶发育,增加植物生物量,强化植物富集效果;增强转运蛋白表达,提高叶面蒸腾作用,促进重金属吸收转运;参与解毒过程,降低重金属毒性,调控重金属体内转化。最后提出了细胞分裂素在重金属污染土壤植物修复中的研究方向,这对促进细胞分裂素在植物修复中的实际应用具有重要意义。 相似文献
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During the past years, major advances have been made in understanding the sequential events involved in neural plate patterning. Positional information is already conferred to cells of the neural plate at the time of its induction in the ectoderm. The interplay between the BMP- and the Fgf- signaling pathways leads to the induction of neural cell fates. Thus, neural induction and neural plate patterning are overlapping processes. Later, at the end of gastrulation, positional cell identities within the neural plate are refined and maintained by the action of several neural plate organizers. By locally emitting signaling molecules, they influence the fate of the developing nervous system with high regional specificity. Recent advances have been made both in understanding the mechanisms that dictate the relative position of these organizers and in how signaling molecules spread from them with high spatial and temporal resolution. 相似文献
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Imai T 《Development, growth & differentiation》2012,54(3):358-365
Positional information is fundamental in development. Although molecular gradients are thought to represent positional information in various systems, the molecular logic used to interpret these gradients remains controversial. In the nervous system, sensory maps are formed in the brain based on gradients of axon guidance molecules. However, it remains unclear how axons find their targets based on relative, not absolute, expression levels of axon guidance receptors. No model solely based on axon-target interactions explains this point. Recent studies in the olfactory system suggested that the neural map formation requires axon-axon interactions, which is known as axon sorting. This review discusses how axon-axon and axon-target interactions interpret molecular gradients and determine the axonal projection sites in neural map formation. 相似文献
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Positional information and pattern formation 总被引:3,自引:0,他引:3
L Wolpert 《Philosophical transactions of the Royal Society of London. Series B, Biological sciences》1981,295(1078):441-450
Spatial patterns of cellular differentiation may arise from cells first being assigned a position, as in a coordinate system, and then interpreting the positional value that they have acquired. This interpretation will depend on their genetic constitution and developmental history. Different patterns may thus arise from similar positional fields. The specification of positional value may involve a positional signal, such as the concentration of a diffusible morphogen, but can also depend on how long the cells remain in a particular region, such as a progress zone. Positional values may also be acquired by direct transfer from one cell layer to another, as in directed embryonic induction. Positional value, unlike a positional signal, involves long-term memory, and can be regarded as a type of cell determination. Cells of the same differentiation class may have different positional values and may thus be non-equivalent. Evidence is presented for a signal providing positional information along the antero-posterior axis during chick limb development. This signal has properties similar to those of a diffusible morphogen. 相似文献
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We have constructed a mutant blocked in the biosynthesis of DIF-1, a chlorinated signal molecule proposed to induce differentiation of both major prestalk cell types formed during Dictyostelium development. Surprisingly, the mutant still forms slugs retaining one prestalk cell type, the pstA cells, and can form mature stalk cells. However, the other major prestalk cell type, the pstO cells, is missing. Normal pstO cell differentiation and their patterning in the slug are restored by development on a uniform concentration of DIF-1. We conclude that pstO and pstA cells are in fact induced by separate signals and that DIF-1 is the pstO inducer. Positional information, in the form of DIF-1 gradients, is evidently not required for pstO cell induction. 相似文献
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Positional information is an important determinant in the establishment of cellular identity in plants. It is established during pattern formation and is maintained in growing organs. Cells maintain the ability to respond to changes in positional information during development indicating that the mechanism for perceiving such information must remain intact until relatively late in development. Once positional cues are perceived they set in motion a number of cascades resulting in the differentiation of particular cell types in defined locations. The circuitry underpinning these later events is being teased out using genetics. Evidence is emerging for the existence of an array of both positive and negative genetic regulators from studies in a number of diverse plant model systems Copyright 1999 Academic Press. 相似文献
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Beutler B 《Current opinion in microbiology》2000,3(1):23-28
Positional cloning work and subsequent biochemical analyses have revealed that Toll-like receptor 4 (Tlr4) transduces the lipopolysaccharide (LPS) signal, alerting the host to infection by Gram-negative bacteria. Moreover, it appears that the LPS sensing pathway is a solitary one: disruption of Tlr4 causes complete unresponsiveness to LPS. As several Tlr family members exist in vertebrates, it appears likely that the innate immune system defends the host by recognizing a small number of structurally conserved molecules that distinguish the microbial world from tissues of the host. 相似文献
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Ratineau C Duluc I Pourreyron C Kedinger M Freund JN Roche C 《Differentiation; research in biological diversity》2003,71(2):163-169
During organogenesis, the intestinal tract progressively acquires a functional regionalization along the antero-posterior axis. Positional information needed for enterocytes has been studied, but the mechanisms that control Paneth and endocrine cell differentiation are poorly understood. We have used a model of endoderm/mesenchyme cross-associations to evaluate the respective roles of endoderm and mesenchyme in the cytodifferentiation of these epithelial cells. Heterotopic cross-associations comprising endoderm and mesenchyme from the presumptive proximal jejunum and colon were developed as xenografts in nude mice. Our results show that endoderm from the presumptive proximal jejunum when associated with colonic mesenchyme generate small intestinal enterocytes. Interestingly, no lysozyme-producing cells were generated. On the other hand, associations comprising colon endoderm and jejunal mesenchyme showed heterodifferentiation with typical small intestinal morphology with sucrase-isomaltase expression and Paneth cell differentiation. Heterotopic associations developed enteroendocrine cell patterns according to the normal fate of the endodermal moiety. As enteroendocrine cell commitment seems to occur before the other intestinal cell types, we cannot exclude a role of instructive signals from the mesenchyme on endocrine cell differentiation earlier in the development. These results identified a complex pattern of cell commitment, dependent of the differentiation type of the epithelial cell, on the regional origin of the endoderm and the associated mesenchyme. 相似文献
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Regenerative medicine has reached the point where we are performing clinical trials with stem-cell-derived cell populations in an effort to treat numerous human pathologies. However, many of these efforts have been challenged by the inability of the engrafted populations to properly integrate into the host environment to make a functional biological unit. It is apparent that we must understand the basic biology of tissue integration in order to apply these principles to the development of regenerative therapies in humans. Studying tissue integration in model organisms, where the process of integration between the newly regenerated tissues and the ‘old’ existing structures can be observed and manipulated, can provide valuable insights. Embryonic and adult cells have a memory of their original position, and this positional information can modify surrounding tissues and drive the formation of new structures. In this Review, we discuss the positional interactions that control the ability of grafted cells to integrate into existing tissues during the process of salamander limb regeneration, and discuss how these insights could explain the integration defects observed in current cell-based regenerative therapies. Additionally, we describe potential molecular tools that can be used to manipulate the positional information in grafted cell populations, and to promote the communication of positional cues in the host environment to facilitate the integration of engrafted cells. Lastly, we explain how studying positional information in current cell-based therapies and in regenerating limbs could provide key insights to improve the integration of cell-based regenerative therapies in the future.KEY WORDS: Integration, Limb regeneration, Positional information, Regenerative medicine, Stem cell 相似文献
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Regulative feedback in pattern formation: towards a general relativistic theory of positional information 总被引:3,自引:0,他引:3
Positional specification by morphogen gradients is traditionally viewed as a two-step process. A gradient is formed and then interpreted, providing a spatial metric independent of the target tissue, similar to the concept of space in classical mechanics. However, the formation and interpretation of gradients are coupled, dynamic processes. We introduce a conceptual framework for positional specification in which cellular activity feeds back on positional information encoded by gradients, analogous to the feedback between mass-energy distribution and the geometry of space-time in Einstein's general theory of relativity. We discuss how such general relativistic positional information (GRPI) can guide systems-level approaches to pattern formation. 相似文献