MICROGLIAL ACTIVATION IN THE INJURED AND HEALTHY BRAIN: WHAT ARE WE REALLY TALKING ABOUT? PRACTICAL AND THEORETICAL ISSUES ASSOCIATED WITH THE MEASUREMENT OF CHANGES IN MICROGLIAL MORPHOLOGY

被引:137
作者
Beynon, S. B.
Walker, F. R. [1 ]
机构
[1] Univ Newcastle, Sch Biomed Sci & Pharm, Lab Affect Neurosci, Callaghan, NSW 2308, Australia
关键词
microglia; morphology; threshold; ramification; reconstruction; IN-VIVO; ALZHEIMERS-DISEASE; RESTING MICROGLIA; MOUSE-BRAIN; CELLS; STRESS; ADULT; MICE; DEGENERATION; LECTIN;
D O I
10.1016/j.neuroscience.2012.07.029
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Recently it has become apparent that microglia play a role not only in responding to insults within the central nervous system but also in responding to changes in synaptic activity and potentially modulating synaptic function. This has led to an enormous expansion of interest in how microglia respond to both pathological and nonpathological challenges, with activities that are associated with unique morphological transformations. Examining changes in microglial morphology can provide direct insight into the cells' functional activities, as morphological status is recognized to be tightly coupled with function. Despite these advances in knowledge, many of the image-based morphometric procedures used to investigate changes in microglial morphology have not kept pace. This has created a situation in which morphometric approaches that have been extensively employed in the past can no longer provide accurate information on the complex transformations that microglia can undergo, particularly under non-pathological conditions. This review critically examines the strengths and weaknesses of existing morphometric analysis procedures. This review further examines efforts to improve the utility of existing approaches and discusses new developments, such as digital reconstruction, that yield more accurate and specific information on how microglia remodel themselves. Ultimately, an improved understanding of the strengths and limitations of existing, and emerging, morphometric approaches will greatly facilitate efforts to understand how microglia remodel themselves in response to the full spectrum of challenges that they are known to encounter. (C) 2012 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:162 / 171
页数:10
相关论文
共 60 条
[1]
Actin-binding proteins coronin-1a and IBA-1 are effective microglial markers for immunohistochemistry [J].
Ahmed, Zeshan ;
Shaw, Gerry ;
Sharma, Ved P. ;
Yang, Cui ;
McGowan, Eileen ;
Dickson, Dennis W. .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2007, 55 (07) :687-700
[2]
Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool [J].
Ajami, Bahareh ;
Bennett, Jami L. ;
Krieger, Charles ;
McNagny, Kelly M. ;
Rossi, Fabio M. V. .
NATURE NEUROSCIENCE, 2011, 14 (09) :1142-U263
[3]
Neuronal 'On' and 'Off' signals control microglia [J].
Biber, Knut ;
Neumann, Harald ;
Inoue, Kazuhide ;
Boddeke, Hendrikus W. G. M. .
TRENDS IN NEUROSCIENCES, 2007, 30 (11) :596-602
[4]
Morphine enhances Tat-induced activation in murine microglia [J].
Bokhari, Sirosh M. ;
Yao, Honghong ;
Bethel-Brown, Crystal ;
Peng Fuwang ;
Williams, Rachel ;
Dhillon, Navneet K. ;
Hegde, Ramakrishna ;
Kumar, Anil ;
Buch, Shilpa J. .
JOURNAL OF NEUROVIROLOGY, 2009, 15 (03) :219-228
[5]
CX3CR1 drives cytotoxic CD4+CD28- T cells into the brain of multiple sclerosis patients [J].
Broux, Bieke ;
Pannemans, Kim ;
Zhang, Xin ;
Markovic-Plese, Silva ;
Broekmans, Tom ;
Eijnde, Bert O. ;
Van Wijmeersch, Bart ;
Somers, Veerle ;
Geusens, Piet ;
van der Pol, Susanne ;
van Horssen, Jack ;
Stinissen, Piet ;
Hellings, Niels .
JOURNAL OF AUTOIMMUNITY, 2012, 38 (01) :10-19
[6]
Caspase signalling controls microglia activation and neurotoxicity [J].
Burguillos, Miguel A. ;
Deierborg, Tomas ;
Kavanagh, Edel ;
Persson, Annette ;
Hajji, Nabil ;
Garcia-Quintanilla, Albert ;
Cano, Josefina ;
Brundin, Patrik ;
Englund, Elisabet ;
Venero, Jose L. ;
Joseph, Bertrand .
NATURE, 2011, 472 (7343) :319-U214
[7]
Low doses of bromo- and iododeoxyuridine produce near-saturation labeling of adult proliferative populations in the dentate gyrus [J].
Burns, KA ;
Kuan, CY .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2005, 21 (03) :803-807
[8]
MORPHOMETRIC ANALYSIS OF MICROGLIA IN ALZHEIMERS-DISEASE [J].
CARPENTER, AF ;
CARPENTER, PW ;
MARKESBERY, WR .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1993, 52 (06) :601-608
[9]
Pathological dynamics of activated microglia following medial forebrain bundle transection [J].
Cho, BP ;
Song, DY ;
Sugama, S ;
Shin, DH ;
Shimizu, Y ;
Kim, SS ;
Kim, YS ;
Joh, TH .
GLIA, 2006, 53 (01) :92-102
[10]
Microglia and the Urokinase Plasminogen Activator Receptor/uPA System in Innate Brain Inflammation [J].
Cunningham, Orla ;
Campion, Suzanne ;
Perry, V. Hugh ;
Murray, Carol ;
Sidenius, Nicolai ;
Docagne, Fabian ;
Cunningham, Colm .
GLIA, 2009, 57 (16) :1802-1814