Quantitating the subtleties of microglial morphology with fractal analysis

被引:372
作者
Karperien, Audrey [1 ]
Ahammer, Helmut [2 ]
Jelinek, Herbert F. [1 ,3 ]
机构
[1] Charles Sturt Univ, Ctr Res Complex Syst, Sch Community Med, Albury, NSW 2640, Australia
[2] Med Univ Graz, Inst Biophys, Graz, Austria
[3] Univ New S Wales, Rural Clin Sch, Sydney, NSW, Australia
关键词
microglia; cell shape; image interpretation: computer-assisted; fractals; models: biological; box counting; lacunarity; multifractal analysis; CENTRAL-NERVOUS-SYSTEM; FETAL CEREBRAL VESSELS; RAT-BRAIN; ALZHEIMERS-DISEASE; OXIDATIVE STRESS; SPINAL-CORD; IN-VITRO; ACTIVATED MICROGLIA; ADHESION MOLECULES; REACTIVE MICROGLIA;
D O I
10.3389/fncel.2013.00003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It is well established that microglial form and function are inextricably linked. In recent years, the traditional view that microglial form ranges between "ramified resting" and "activated amoeboid" has been emphasized through advancing imaging techniques that point to microglial form being highly dynamic even within the currently accepted morphological categories. Moreover, microglia adopt meaningful intermediate forms between categories, with considerable crossover in function and varying morphologies as they cycle, migrate, wave, phagocytose, and extend and retract fine and gross processes. From a quantitative perspective, it is problematic to measure such variability using traditional methods, but one way of quantitating such detail is through fractal analysis. The techniques of fractal analysis have been used for quantitating microglial morphology, to categorize gross differences but also to differentiate subtle differences (e.g., amongst ramified cells). Multifractal analysis in particular is one technique of fractal analysis that may be useful for identifying intermediate forms. Here we review current trends and methods of fractal analysis, focusing on box counting analysis, including lacunarity and multifractal analysis, as applied to microglial morphology.
引用
收藏
页码:1 / 34
页数:18
相关论文
共 171 条
[1]   Migration and differentiation of neural precursor cells can be directed by microglia [J].
Aarum, J ;
Sandberg, K ;
Haeberlein, SLB ;
Persson, MAA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (26) :15983-15988
[2]   Higuchi Dimension of Digital Images [J].
Ahammer, Helmut .
PLOS ONE, 2011, 6 (09)
[3]   Microglia derive from progenitors, originating from the yolk sac, and which proliferate in the brain [J].
Alliot, F ;
Godin, I ;
Pessac, B .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 117 (02) :145-152
[4]   Macrophages/microglial cells in human central nervous system during development: an immunohistochemical study [J].
Andjelkovic, AV ;
Nikolic, B ;
Pachter, JS ;
Zecevic, N .
BRAIN RESEARCH, 1998, 814 (1-2) :13-25
[5]  
[Anonymous], 1983, FRACTAL GEOMETRY NAT
[6]   Hypoxia and Oxidative Stress in the Causation of Diabetic Retinopathy [J].
Arden, Geoffrey B. ;
Sivaprasad, Sobha .
CURRENT DIABETES REVIEWS, 2011, 7 (05) :291-304
[7]   Cognition network technology:: Object orientation and fractal topology in biomedical image analysis -: Method and applications [J].
Baatz, M ;
Schäpe, A ;
Schmidt, G ;
Athelogou, M ;
Binnig, G .
Fractals in Biology and Medicine, Vol IV, 2005, :67-73
[8]   Image resolution and exposure time of digital radiographs affects fractal dimension of periapical bone [J].
Baksi, B. Guniz ;
Fidler, Ales .
CLINICAL ORAL INVESTIGATIONS, 2012, 16 (05) :1507-1510
[9]   [11C](R)-PK11195 positron emission tomography imaging of activated microglia in vivo in Rasmussen's encephalitis [J].
Banati, RB ;
Goerres, GW ;
Myers, R ;
Gunn, RN ;
Turkheimer, FE ;
Kreutzberg, GW ;
Brooks, DJ ;
Jones, T ;
Duncan, JS .
NEUROLOGY, 1999, 53 (09) :2199-2203
[10]   Evidence for activation of microglia in patients with psychiatric illnesses [J].
Bayer, TA ;
Buslei, R ;
Havas, L ;
Falkai, P .
NEUROSCIENCE LETTERS, 1999, 271 (02) :126-128