hliu092 发表于 2021-1-5 10:36:51

The 'Thoughts' of Cell/细胞的思维

This is the article 11 in the theme 'Environmental Physiology/环境生理学' of Journal of Environment and Health Science.

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hliu092 发表于 2021-1-6 10:26:23

Article 11. Assimilation of The Cells ‘Thoughts’ Between Different Phenotypes and Its Implication on Canceration/ 不同表现型细胞间在‘思维’上的的同化机制及在癌变过程的指示意义

Author: Liu Huan, MSc (First Class Honours), The University of Auckland. Published after graduation on 21/01/2016

Methods:
As described in other articles of this journal, after UV-B simulation process stops, both sample 1 and sample 2 of the same genetic strain are transferred into moisture simulation process.

Step 1. Both sample 1 and sample 2 are cultivated separately and individually in each moisture simulation process (T1, T2, ..., Tn);

Step 2. The samples of even mixture between sample 1 and sample 2 (50% for each sample) are cultivated individually in each moisture simulation process (T1, T2, ..., Tn) as well; The cultivation condition is the same between step 1 and step 2, and step 1 and step 2 is conducted independently;

Step 3. The reproduction rate (or cell division rate) is observed, and the comparison of cell division rates between step 1 and step 2 under the same cultivation condition is conducted: in step 1, the cell division rate of sample 1 and sample 2 is R1 (cell quantity/time) and R2, respectively; if assimilation of the cells’ ‘memory’ does NOT occur, then the cell division rate of mixture sample is 0.5*(R1+R2); however, if assimilation of the cells’ ‘memory’ does occur, then the cell division rate of mixture sample is not equivalent to 0.5*(R1+R2); if the cell division rate of mixture sample is closer to R1, the sample 1 becomes dominant; if the cell division rate of mixture sample is closer to R2, the sample 2 becomes dominant.


Discussion:

Within the cells of the same genetic strain, cells apparently assimilate each other between different phenotypes. It is expected that sample 1 tends to be dominantduring comfortable condition; and sample 2 tends to be dominant during adverse conditions. This theory is applicable on the cancerous tissue: when cancerous cell without immunology becomes dominant in cell assimilation process, the whole tissue (or organ) starts to be canceration, so the prevention of cancerous cell assimilation is the key in pathological study. Appendix of this chapter lists the experiment procedure for blood cell cultivation, further support the discussion of this chapter.
Appendix. The simulation methods for blood cell cultivation

As described by other articles of this journal, after electromagnetism simulation for cell cultivation process stops, both blood sample 1 and sample 2 of arat (or the same genetic strain) are transferred into simulation process of physiological saline:

Step 1. Simulation process of physiological saline: cells are cultivated individually in different concentrations of physiological saline in Lab, and different cell environment (salinity stress of cell environment or ‘thirsty’ simulation) are labeled as T1, T2, ..., Tn.

Step 2. The samples of even mixture between sample 1 and sample 2 are cultivated individually in each different concentrations of physiological saline (T1, T2, ..., Tn) as well; The cultivation condition for blood cell is the same between step 1 and step 2, and step 1 and step 2 is conducted independently.

The other steps are the same as described above. To be continued...


This is the revised materials in book “Proceedings for Degree of Postgraduate Diploma in Environmental Science (3rd Edition).” Published in 2016. The ‘chapter’ content mentioned in this article is in previous book. Revised on 05/01/2021.

References:
All the science terms in English of this journal source from Wikipedia:
https://encyclopedia.thefreedictionary.com/;
本文所有中文科学专业术语引用自百度百科 https://baike.baidu.com/。

hliu092 发表于 2021-1-5 10:37:19

Article 11. Assimilation of The Cells’ ‘Memory’ Between Different Phenotypes and Its Implication on Canceration/ 不同表现型细胞间在‘思维’上的的同化机制及在癌变过程的指示意义
Author: Liu Huan, MSc (First Class Honours), The University of Auckland. Published after graduation on 21/01/2016

Methods:
As described in chapter 9 in this book, after UV-B simulation process stops, both sample 1 and sample 2 of the same genetic strain are transferred into moisture simulation process.

Step 1. Both sample 1 and sample 2 are cultivated separately and individually in each moisture simulation process (T1, T2, ..., Tn);

Step 2. The samples of even mixture between sample 1 and sample 2 (50% for each sample) are cultivated individually in each moisture simulation process (T1, T2, ..., Tn) as well; The cultivation condition is the same between step 1 and step 2, and step 1 and step 2 is conducted independently;

Step 3. The reproduction rate (or cell division rate) is observed, and the comparison of cell division rates between step 1 and step 2 under the same cultivation condition is conducted: in step 1, the cell division rate of sample 1 and sample 2 is R1 (cell quantity/time) and R2, respectively; if assimilation of the cells’ ‘memory’ does NOT occur, then the cell division rate of mixture sample is 0.5*(R1+R2); however, if assimilation of the cells’ ‘memory’ does occur, then the cell division rate of mixture sample is not equivalent to 0.5*(R1+R2); if the cell division rate of mixture sample is closer to R1, the sample 1 becomes dominant; if the cell division rate of mixture sample is closer to R2, the sample 2 becomes dominant.


Discussion:

Within the cells of the same genetic strain, cells apparently assimilate each other between different phenotypes. It is expected that sample 1 tends to be dominantduring comfortable condition; and sample 2 tends to be dominant during adverse conditions. This theory is applicable on the cancerous tissue: when cancerous cell without immunology becomes dominant in cell assimilation process, the whole tissue (or organ) starts to be canceration, so the prevention of cancerous cell assimilation is the key in pathological study. Appendix of this chapter lists the experiment procedure for blood cell cultivation, further support the discussion of this chapter.

Appendix. The simulation methods for blood cell cultivation

As described by the appendix of chapter 9 in this book, after electromagnetism simulation for cell cultivation process stops, both blood sample 1 and sample 2 of arat (or the same genetic strain) are transferred into simulation process of physiological saline:

Step 1. Simulation process of physiological saline: cells are cultivated individually in different concentrations of physiological saline in Lab, and different cell environment (salinity stress of cell environment or ‘thirsty’ simulation) are labeled as T1, T2, ..., Tn.

Step 2. The samples of even mixture between sample 1 and sample 2 are cultivated individually in each different concentrations of physiological saline (T1, T2, ..., Tn) as well; The cultivation condition for blood cell is the same between step 1 and step 2, and step 1 and step 2 is conducted independently.

The other steps are the same as described above. To be continued...
This is the revised materials in book “Proceedings for Degree of Postgraduate Diploma in Environmental Science (3rd Edition).” published in 2016. Revised on 05/01/2021.

References: the conceptions and terms of biology in this book sources from Wikipedia,
the free encyclopedia.

hliu092 发表于 2021-1-5 11:09:33

Article 11. Assimilation of The Cells’ ‘Memory’ Between Different Phenotypes and Its Implication on Canceration/ 不同表现型细胞间在‘思维’上的的同化机制及在癌变过程的指示意义

Author: Liu Huan, MSc (First Class Honours), The University of Auckland. Published after graduation on 21/01/2016

Methods:
As described in other articles of this journal, after UV-B simulation process stops, both sample 1 and sample 2 of the same genetic strain are transferred into moisture simulation process.

Step 1. Both sample 1 and sample 2 are cultivated separately and individually in each moisture simulation process (T1, T2, ..., Tn);

Step 2. The samples of even mixture between sample 1 and sample 2 (50% for each sample) are cultivated individually in each moisture simulation process (T1, T2, ..., Tn) as well; The cultivation condition is the same between step 1 and step 2, and step 1 and step 2 is conducted independently;

Step 3. The reproduction rate (or cell division rate) is observed, and the comparison of cell division rates between step 1 and step 2 under the same cultivation condition is conducted: in step 1, the cell division rate of sample 1 and sample 2 is R1 (cell quantity/time) and R2, respectively; if assimilation of the cells’ ‘memory’ does NOT occur, then the cell division rate of mixture sample is 0.5*(R1+R2); however, if assimilation of the cells’ ‘memory’ does occur, then the cell division rate of mixture sample is not equivalent to 0.5*(R1+R2); if the cell division rate of mixture sample is closer to R1, the sample 1 becomes dominant; if the cell division rate of mixture sample is closer to R2, the sample 2 becomes dominant.


Discussion:

Within the cells of the same genetic strain, cells apparently assimilate each other between different phenotypes. It is expected that sample 1 tends to be dominantduring comfortable condition; and sample 2 tends to be dominant during adverse conditions. This theory is applicable on the cancerous tissue: when cancerous cell without immunology becomes dominant in cell assimilation process, the whole tissue (or organ) starts to be canceration, so the prevention of cancerous cell assimilation is the key in pathological study. Appendix of this chapter lists the experiment procedure for blood cell cultivation, further support the discussion of this chapter.

Appendix. The simulation methods for blood cell cultivation

As described by other articles of this journal, after electromagnetism simulation for cell cultivation process stops, both blood sample 1 and sample 2 of arat (or the same genetic strain) are transferred into simulation process of physiological saline:

Step 1. Simulation process of physiological saline: cells are cultivated individually in different concentrations of physiological saline in Lab, and different cell environment (salinity stress of cell environment or ‘thirsty’ simulation) are labeled as T1, T2, ..., Tn.

Step 2. The samples of even mixture between sample 1 and sample 2 are cultivated individually in each different concentrations of physiological saline (T1, T2, ..., Tn) as well; The cultivation condition for blood cell is the same between step 1 and step 2, and step 1 and step 2 is conducted independently.

The other steps are the same as described above. To be continued...


This is the revised materials in book “Proceedings for Degree of Postgraduate Diploma in Environmental Science (3rd Edition).” published in 2016. Revised on 05/01/2021.

References: the conceptions and terms of biology in this book sources from Wikipedia, the free encyclopedia.
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