Literature DB >> 24468477

High-resolution intravital imaging reveals that blood-derived macrophages but not resident microglia facilitate secondary axonal dieback in traumatic spinal cord injury.

Teresa A Evans1, Deborah S Barkauskas2, Jay T Myers3, Elisabeth G Hare4, Jing Qiang You5, Richard M Ransohoff6, Alex Y Huang7, Jerry Silver8.   

Abstract

After traumatic spinal cord injury, functional deficits increase as axons die back from the center of the lesion and the glial scar forms. Axonal dieback occurs in two phases: an initial axon intrinsic stage that occurs over the first several hours and a secondary phase which takes place over the first few weeks after injury. Here, we examine the secondary phase, which is marked by infiltration of macrophages. Using powerful time-lapse multi-photon imaging, we captured images of interactions between Cx3cr1(+/GFP) macrophages and microglia and Thy-1(YFP) axons in a mouse dorsal column crush spinal cord injury model. Over the first few weeks after injury, axonal retraction bulbs within the lesion are static except when axonal fragments are lost by a blebbing mechanism in response to physical contact followed by phagocytosis by mobile Cx3Cr1(+/GFP) cells. Utilizing a radiation chimera model to distinguish marrow-derived cells from radio-resistant CNS-resident microglia, we determined that the vast majority of accumulated cells in the lesion are derived from the blood and only these are associated with axonal damage. Interestingly, CNS-resident Cx3Cr1(+/GFP) microglia did not increasingly accumulate nor participate in neuronal destruction in the lesion during this time period. Additionally, we found that the blood-derived cells consisted mainly of singly labeled Ccr2(+/RFP) macrophages, singly labeled Cx3Cr1(+/GFP) macrophages and a small population of double-labeled cells. Since all axon destructive events were seen in contact with a Cx3Cr1(+/GFP) cell, we infer that the CCR2 single positive subset is likely not robustly involved in axonal dieback. Finally, in our model, deletion of CCR2, a chemokine receptor, did not alter the position of axons after dieback. Understanding the in vivo cellular interactions involved in secondary axonal injury may lead to clinical treatment candidates involving modulation of destructive infiltrating blood monocytes.
Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Axonal dieback; Bone marrow chimera mice; CCR2; CX3CR1; Macrophages; Microglia; Monocytes; Retraction bulb; Spinal cord injury; Two-photon microscopy

Mesh:

Substances:

Year:  2014        PMID: 24468477      PMCID: PMC3954731          DOI: 10.1016/j.expneurol.2014.01.013

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  56 in total

1.  Regulation of tau pathology by the microglial fractalkine receptor.

Authors:  Kiran Bhaskar; Megan Konerth; Olga N Kokiko-Cochran; Astrid Cardona; Richard M Ransohoff; Bruce T Lamb
Journal:  Neuron       Date:  2010-10-06       Impact factor: 17.173

2.  CX3CR1 deficiency alters microglial activation and reduces beta-amyloid deposition in two Alzheimer's disease mouse models.

Authors:  Sungho Lee; Nicholas H Varvel; Megan E Konerth; Guixiang Xu; Astrid E Cardona; Richard M Ransohoff; Bruce T Lamb
Journal:  Am J Pathol       Date:  2010-09-23       Impact factor: 4.307

3.  The unusual response of serotonergic neurons after CNS Injury: lack of axonal dieback and enhanced sprouting within the inhibitory environment of the glial scar.

Authors:  Alicia L Hawthorne; Hongmei Hu; Bornali Kundu; Michael P Steinmetz; Christi J Wylie; Evan S Deneris; Jerry Silver
Journal:  J Neurosci       Date:  2011-04-13       Impact factor: 6.167

4.  Deficient CX3CR1 signaling promotes recovery after mouse spinal cord injury by limiting the recruitment and activation of Ly6Clo/iNOS+ macrophages.

Authors:  Dustin J Donnelly; Erin E Longbrake; Todd M Shawler; Kristina A Kigerl; Wenmin Lai; C Amy Tovar; Richard M Ransohoff; Phillip G Popovich
Journal:  J Neurosci       Date:  2011-07-06       Impact factor: 6.167

Review 5.  Repertoire of microglial and macrophage responses after spinal cord injury.

Authors:  Samuel David; Antje Kroner
Journal:  Nat Rev Neurosci       Date:  2011-06-15       Impact factor: 34.870

6.  Fate mapping analysis reveals that adult microglia derive from primitive macrophages.

Authors:  Florent Ginhoux; Melanie Greter; Marylene Leboeuf; Sayan Nandi; Peter See; Solen Gokhan; Mark F Mehler; Simon J Conway; Lai Guan Ng; E Richard Stanley; Igor M Samokhvalov; Miriam Merad
Journal:  Science       Date:  2010-10-21       Impact factor: 47.728

7.  A mouse model of in utero transplantation.

Authors:  Amar Nijagal; Tom Le; Marta Wegorzewska; Tippi C Mackenzie
Journal:  J Vis Exp       Date:  2011-01-27       Impact factor: 1.355

8.  Adult NG2+ cells are permissive to neurite outgrowth and stabilize sensory axons during macrophage-induced axonal dieback after spinal cord injury.

Authors:  Sarah A Busch; Kevin P Horn; Fernando X Cuascut; Alicia L Hawthorne; Lianhua Bai; Robert H Miller; Jerry Silver
Journal:  J Neurosci       Date:  2010-01-06       Impact factor: 6.167

9.  Selective chemokine receptor usage by central nervous system myeloid cells in CCR2-red fluorescent protein knock-in mice.

Authors:  Noah Saederup; Astrid E Cardona; Kelsey Croft; Makiko Mizutani; Anne C Cotleur; Chia-Lin Tsou; Richard M Ransohoff; Israel F Charo
Journal:  PLoS One       Date:  2010-10-27       Impact factor: 3.240

10.  Fractalkine receptor (CX3CR1) deficiency sensitizes mice to the behavioral changes induced by lipopolysaccharide.

Authors:  Angela W Corona; Yan Huang; Jason C O'Connor; Robert Dantzer; Keith W Kelley; Phillip G Popovich; Jonathan P Godbout
Journal:  J Neuroinflammation       Date:  2010-12-17       Impact factor: 8.322

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  93 in total

Review 1.  Central nervous system myeloid cells as drug targets: current status and translational challenges.

Authors:  Knut Biber; Thomas Möller; Erik Boddeke; Marco Prinz
Journal:  Nat Rev Drug Discov       Date:  2015-12-04       Impact factor: 84.694

Review 2.  The role of the microglia in acute CNS injury.

Authors:  Masahito Kawabori; Midori A Yenari
Journal:  Metab Brain Dis       Date:  2014-03-29       Impact factor: 3.584

3.  A surviving intact branch stabilizes remaining axon architecture after injury as revealed by in vivo imaging in the mouse spinal cord.

Authors:  Ariana O Lorenzana; Jae K Lee; Matthew Mui; Amy Chang; Binhai Zheng
Journal:  Neuron       Date:  2015-04-30       Impact factor: 17.173

4.  Olfactory Ensheathing Cell Transplantation after a Complete Spinal Cord Transection Mediates Neuroprotective and Immunomodulatory Mechanisms to Facilitate Regeneration.

Authors:  Rana R Khankan; Khris G Griffis; James R Haggerty-Skeans; Hui Zhong; Roland R Roy; V Reggie Edgerton; Patricia E Phelps
Journal:  J Neurosci       Date:  2016-06-08       Impact factor: 6.167

5.  In vivo dynamics of retinal microglial activation during neurodegeneration: confocal ophthalmoscopic imaging and cell morphometry in mouse glaucoma.

Authors:  Alejandra Bosco; Cesar O Romero; Balamurali K Ambati; Monica L Vetter
Journal:  J Vis Exp       Date:  2015-05-11       Impact factor: 1.355

Review 6.  Central nervous system regenerative failure: role of oligodendrocytes, astrocytes, and microglia.

Authors:  Jerry Silver; Martin E Schwab; Phillip G Popovich
Journal:  Cold Spring Harb Perspect Biol       Date:  2014-12-04       Impact factor: 10.005

Review 7.  Elucidation of monocyte/macrophage dynamics and function by intravital imaging.

Authors:  Rejane Rua; Dorian B McGavern
Journal:  J Leukoc Biol       Date:  2015-07-10       Impact factor: 4.962

8.  Spinal Motor Circuit Synaptic Plasticity after Peripheral Nerve Injury Depends on Microglia Activation and a CCR2 Mechanism.

Authors:  Travis M Rotterman; Erica T Akhter; Alicia R Lane; Kathryn P MacPherson; Violet V García; Malú G Tansey; Francisco J Alvarez
Journal:  J Neurosci       Date:  2019-03-04       Impact factor: 6.167

Review 9.  The origin, fate, and contribution of macrophages to spinal cord injury pathology.

Authors:  Lindsay M Milich; Christine B Ryan; Jae K Lee
Journal:  Acta Neuropathol       Date:  2019-03-30       Impact factor: 17.088

Review 10.  Inflammatory reaction after traumatic brain injury: therapeutic potential of targeting cell-cell communication by chemokines.

Authors:  Stefka Gyoneva; Richard M Ransohoff
Journal:  Trends Pharmacol Sci       Date:  2015-05-13       Impact factor: 14.819

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