2013
DOI: 10.1002/lsm.22133
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808 nm Wavelength Light Induces a Dose‐Dependent Alteration in Microglial Polarization and Resultant Microglial Induced Neurite Growth

Abstract: These data suggest that the Arndt-Schulz law as applied to PBM for a specific bioassay does not hold true in cells with a spectrum of responses, and that PBM can alter microglial phenotype across this spectrum in a dose-dependent manner. These data are therefore of important relevance to not only therapies in the CNS but also to understanding of PBM effects and mechanisms.

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Cited by 48 publications
(47 citation statements)
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“…While others have demonstrated the impact of wavelength and dose on inflammatory cells in vitro [37, 53], to our knowledge, we are the first to demonstrate the effect of 670 nm light on the polarization of activated microglia/macrophages following spinal cord injury in vivo. The pattern and sequence of pro-inflammatory M1 (CD80 + ED1 + ) cell activation, cell death, followed by anti-inflammatory/wound-healing M2 (Arginase1 + ED1 + ) recruitment observed in sham-treated animals in our study is consistent with what is expected under conditions of spinal cord injury and repair [30, 31].…”
Section: Discussionmentioning
confidence: 70%
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“…While others have demonstrated the impact of wavelength and dose on inflammatory cells in vitro [37, 53], to our knowledge, we are the first to demonstrate the effect of 670 nm light on the polarization of activated microglia/macrophages following spinal cord injury in vivo. The pattern and sequence of pro-inflammatory M1 (CD80 + ED1 + ) cell activation, cell death, followed by anti-inflammatory/wound-healing M2 (Arginase1 + ED1 + ) recruitment observed in sham-treated animals in our study is consistent with what is expected under conditions of spinal cord injury and repair [30, 31].…”
Section: Discussionmentioning
confidence: 70%
“…However, wavelength (i.e. 660 vs. 780 nm) has been shown to alter the expression of inflammatory mediators expressed by activated pro-inflammatory microglia/macrophages [37], and light dosage has been shown to alter the balance of M1/M2 cell expression [53]. These in vitro studies suggest that other mechanisms, unrelated to cytochrome C oxidase, may influence the inflammatory microenvironment following light treatment.…”
Section: Discussionmentioning
confidence: 99%
“…The effects of PBM on macrophage phenotypes are beginning to be described in cell cultures studies,10, 30, 31, 32, 33, 34 evidencing that this therapeutic modality, especially using the NIR wavelength, is capable of altering the polarization of these cells in vitro. In vivo experiments have demonstrated that PBM (808 nm) can shift the phenotype of brain microglial polarization from the pro‐inflammatory phenotype (M1) to the anti‐inflammatory (M2) phenotype after ischemic stroke, promoting cortical neurogenesis 35.…”
Section: Discussionmentioning
confidence: 99%
“…[30][31][32] Moreover, in vivo and in vitro studies have shown that exposure to light causes changes in inflammatory cell migration into the injured spinal cord [33][34][35][36] and modulates microglia polarization from a proinflammatory to anti-inflammatory phenotype. 37 After peripheral (sciatic) nerve injury, the transcutaneous application of laser light over the corresponding segment of the spinal cord improved measures of nerve function and neurologic recovery in rats, compared with values for (non-laser-light-treated) controls. 38,39 To the author's knowledge, only 2 clinical trials on photobiomodulation therapy in dogs with naturally occurring SCI have been conducted.…”
Section: Ivddmentioning
confidence: 98%