Computational physiology and the physiome project

被引:133
作者
Crampin, EJ
Halstead, M
Hunter, P
Nielsen, P
Noble, D
Smith, N
Tawhai, M
机构
[1] Univ Auckland, Bioengn Inst, Auckland 1, New Zealand
[2] Univ Oxford, Inst Math, Ctr Math Biol, Oxford OX1 3LB, England
[3] Univ Oxford, Physiol Lab, Oxford OX1 3PT, England
关键词
D O I
10.1113/expphysiol.2003.026740
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Bioengineering analyses of physiological systems use the computational solution of physical conservation laws on anatomically detailed geometric models to understand the physiological function of intact organs in terms of the properties and behaviour of the cells and tissues within the organ. By linking behaviour in a quantitative, mathematically defined sense across multiple scales of biological organization - from proteins to cells, tissues, organs and organ systems - these methods have the potential to link patient-specific knowledge at the two ends of these spatial scales. A genetic profile linked to cardiac ion channel mutations, for example, can be interpreted in relation to body surface ECG measurements via a mathematical model of the heart and torso, which includes the spatial distribution of cardiac ion channels throughout the myocardium and the individual kinetics for each of the approximately 50 types of ion channel, exchanger or pump known to be present in the heart. Similarly, linking molecular defects such as mutations of chloride ion channels in lung epithelial cells to the integrated function of the intact lung requires models that include the detailed anatomy of the lungs, the physics of air flow, blood flow and gas exchange, together with the large deformation mechanics of breathing. Organizing this large body of knowledge into a coherent framework for modelling requires the development of ontologies, markup languages for encoding models, and web-accessible distributed databases. In this article we review the state of the field at all the relevant levels, and the tools that are being developed to tackle such complexity. Integrative physiology is central to the interpretation of genomic and proteomic data, and is becoming a highly quantitative, computer-intensive discipline.
引用
收藏
页码:1 / 26
页数:26
相关论文
共 120 条
[21]  
Dawkins R., 1976, SELFISH GENE
[22]   The brave new world of RNA [J].
Dennis, C .
NATURE, 2002, 418 (6894) :122-124
[23]   A mathematical model for the morphology of the pulmonary acinus [J].
Denny, E ;
Schroter, RC .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1996, 118 (02) :210-215
[24]  
Diamond Jared, 1993, P89
[25]   A MODEL OF CARDIAC ELECTRICAL-ACTIVITY INCORPORATING IONIC PUMPS AND CONCENTRATION CHANGES [J].
DIFRANCESCO, D ;
NOBLE, D .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1985, 307 (1133) :353-398
[26]   TOTAL EXCITATION OF ISOLATED HUMAN HEART [J].
DURRER, D ;
VANDAM, RT ;
FREUD, GE ;
JANSE, MJ ;
MEIJLER, FL ;
ARZBAECHER, RC .
CIRCULATION, 1970, 41 (06) :899-+
[27]   A human acinar structure for simulation of realistic alveolar plateau slopes [J].
Dutrieue, B ;
Vanholsbeeck, F ;
Verbanck, S ;
Paiva, M .
JOURNAL OF APPLIED PHYSIOLOGY, 2000, 89 (05) :1859-1867
[28]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[29]   A synthetic oscillatory network of transcriptional regulators [J].
Elowitz, MB ;
Leibler, S .
NATURE, 2000, 403 (6767) :335-338
[30]   Laser capture microdissection [J].
EmmertBuck, MR ;
Bonner, RF ;
Smith, PD ;
Chuaqui, RF ;
Zhuang, ZP ;
Goldstein, SR ;
Weiss, RA ;
Liotta, LA .
SCIENCE, 1996, 274 (5289) :998-1001