Jaross Werner
Institute of Clinical Chemistry and Laboratory Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Fetscherstrasse 74, 01307 Dresden, Germany.
Open Biochem J. 2016 Mar 22;10:12-6. doi: 10.2174/1874091X01610010012. eCollection 2016.
To date the manner in which information reaches the nucleus on that part within the three-dimensional structure where specific restorative processes of structural components of the cell are required is unknown. The soluble signalling molecules generated in the course of destructive and restorative processes communicate only as needed.
All molecules show temperature-dependent molecular vibration creating a radiation in the infrared region. Each molecule species has in its turn a specific frequency pattern under given specific conditions. Changes in their structural composition result in modified frequency patterns of the molecules in question. The main structural elements of the cell membrane, of the endoplasmic reticulum, of the Golgi apparatus, and of the different microsomes representing the great variety of polar lipids show characteristic frequency patterns with peaks in the region characterised by low water absorption. These structural elements are very dynamic, mainly caused by the creation of signal molecules and transport containers. By means of the characteristic radiation, the area where repair or substitution services are needed could be identified; this spatial information complements the signalling of the soluble signal molecules. Based on their resonance properties receptors located on the outer leaflet of the nuclear envelope should be able to read typical frequencies and pass them into the nucleus. Clearly this physical signalling must be blocked by the cell membrane to obviate the flow of information into adjacent cells.
If the hypothesis can be proved experimentally, it should be possible to identify and verify characteristic infrared frequency patterns. The application of these signal frequencies onto cells would open entirely new possibilities in medicine and all biological disciplines specifically to influence cell growth and metabolism. Similar to this intracellular system, an extracellular signalling system with many new therapeutic options has to be discussed.
迄今为止,在细胞结构成分的特定修复过程所需的三维结构部分,信息到达细胞核的方式尚不清楚。在破坏和修复过程中产生的可溶性信号分子仅在需要时进行通讯。
所有分子都表现出与温度相关的分子振动,从而在红外区域产生辐射。在给定的特定条件下,每种分子都有其特定的频率模式。它们结构组成的变化会导致相关分子的频率模式发生改变。细胞膜、内质网、高尔基体以及代表各种极性脂质的不同微粒体的主要结构元素,在低吸水区域具有特征性频率模式峰值。这些结构元素非常动态,主要是由信号分子和运输容器的产生引起的。通过特征辐射,可以识别需要修复或替换服务的区域;这种空间信息补充了可溶性信号分子的信号传递。基于其共振特性,位于核膜外小叶上的受体应该能够读取典型频率并将其传递到细胞核中。显然,这种物理信号必须被细胞膜阻断,以避免信息流入相邻细胞。
如果该假设能够通过实验得到证明,那么应该有可能识别和验证特征性红外频率模式。将这些信号频率应用于细胞将在医学和所有生物学科中开辟全新的可能性,特别是影响细胞生长和代谢。与这种细胞内系统类似,必须讨论一种具有许多新治疗选择的细胞外信号系统。