Physiological Models

1988 ◽  
pp. 265-282
Author(s):  
Jack George Thompson
Keyword(s):  
Author(s):  
F Tardieu ◽  
I S C Granato ◽  
E J Van Oosterom ◽  
B Parent ◽  
G L Hammer

Abstract Tailoring genotypes for the variety of environmental scenarios associated with climate change requires modelling of the genetic variability of adaptation mechanisms to environmental cues. A large number of physiological mechanisms have been described and modelled, e.g. at transcript, metabolic or hormonal levels, but they remain to be assembled into whole-plant and canopy models. A 'bottom-up' approach combining physiological mechanisms leads to a near-infinite number of combinations and to an unmanageable number of parameters, so more parsimonious approaches are required. We propose that natural selection has constrained the large diversity of mechanisms into consistent strategies, in such a way that not all combinations of mechanisms are possible. These constraints, and resulting feedbacks, result in integrative 'metamechanisms', e.g. response curves of traits to environmental conditions, measurable via high throughput phenotyping, and resulting in robust and stable equations with heritable genotype-dependent parameters. Examples are provided for the responses of developmental traits to temperature, for the response of growth and yield to water deficit and evaporative demand, and for the response of tillering to light and temperature. In these examples, it was inoperative to combine upstream mechanisms into whole-plant mechanisms, whereas the evolutionary constraints on the combinations of physiological mechanisms renders possible the use of genotype-specific response curves at plant or canopy levels. These can be used for a new generation of crop models capable of simulating the behavior of thousands of genotypes. This has significant consequences for plant modelling and its use in genetics and breeding.


2021 ◽  
pp. 113833
Author(s):  
David Olmeda ◽  
Daniela Cerezo-Wallis ◽  
Elena Castellano-Sanz ◽  
Susana García-Silva ◽  
Héctor Peinado ◽  
...  

Lab on a Chip ◽  
2015 ◽  
Vol 15 (3) ◽  
pp. 614-636 ◽  
Author(s):  
Qasem Ramadan ◽  
Martin A. M. Gijs
Keyword(s):  

We review the recent development in functional microphysiological models and present an outlook on the opportunities for translational development in immunology.


2016 ◽  
Vol 57 (3-4) ◽  
pp. 224-239 ◽  
Author(s):  
Franziska Mußbach ◽  
Utz Settmacher ◽  
Olaf Dirsch ◽  
Chichi Xie ◽  
Uta Dahmen

Background: Organ engineering is a new innovative strategy to cope with two problems: the need for physiological models for pharmacological research and donor organs for transplantation. A functional scaffold is generated from explanted organs by removing all cells (decellularization) by perfusing the organ with ionic or nonionic detergents via the vascular system. Subsequently the acellular scaffold is reseeded with organ-specific cells (repopulation) to generate a functional organ. Summary: This review gives an overview of the state of the art describing the decellularization process, the subsequent quality assessment, the repopulation techniques and the functional assessment. It emphasizes the use of scaffolds as matrix for culturing human liver cells for drug testing. Further, it highlights the techniques for transplanting these engineered scaffolds in allogeneic or xenogeneic animals in order to test their biocompatibility and use as organ grafts. Key Messages: The first issue is the so-called decellularization, which is best explored and resulted in a multitude of different protocols. The most promising approach seems to be the combination of pulsatile perfusion of the liver with Triton X-100 and SDS via hepatic artery and portal vein. Widely accepted parameters of quality control include the quantitative assessment of the DNA content and the visualization of eventually remaining nuclei confirmed by HE staining. Investigations regarding the composition of the extracellular matrix focused on histological determination of laminin, collagen, fibronectin and elastin and remained qualitatively. Repopulation is the second issue which is addressed. Selection of the most suitable cell type is a highly controversial topic. Currently, the highest potential is seen for progenitor and stem cells. Cells are infused into the scaffold and cultured under static conditions or in a bioreactor allowing dynamic perfusion of the scaffold. The quality of repopulation is mainly assessed by routine histology and basic functional assays. These promising results prompted to consider the use of a liver scaffold repopulated with human cells for pharmacological research. Transplantation of the (repopulated) scaffold is the third topic which is not yet widely addressed. Few studies report the heterotopic transplantation of repopulated liver tissue without vascular anastomosis. Even fewer studies deal with the heterotopic transplantation of a scaffold or a repopulated liver lobe. However, observation time was still limited to hours, and long-term graft survival has not been reported yet. These exciting results emphasize the potential of this new and promising strategy to create physiological models for pharmacological research and to generate liver grafts for the transplant community to treat organ failure. However, the scientific need for further development in the field of liver engineering is still tremendous.


2000 ◽  
Vol 90 (3) ◽  
pp. 614-618 ◽  
Author(s):  
Jonathan G. Hardman ◽  
Jonathan S. Wills ◽  
Alan R. Aitkenhead
Keyword(s):  

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