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Beneficial effects of secretory leukocyte protease inhibitor after spinal cord injury

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TLDR
It is shown that recombinant secretory leukocyte protease inhibitor injected intraperitoneally localizes to the nucleus of circulating leukocytes, is detected in the injured spinal cord, reduces activation of nuclear factor-kappaB and expression of tumour necrosis factor-alpha, and might be useful for the treatment of acute spinal cord injury.
Abstract
Secretory leukocyte protease inhibitor is a serine protease inhibitor produced by various cell types, including neutrophils and activated macrophages, and has anti-inflammatory properties. It has been shown to promote wound healing in the skin and other non-neural tissues, however, its role in central nervous system injury was not known. We now report a beneficial role for secretory leukocyte protease inhibitor after spinal cord injury. After spinal cord contusion injury in mice, secretory leukocyte protease inhibitor is expressed primarily by astrocytes and neutrophils but not macrophages. We show, using transgenic mice over-expressing secretory leukocyte protease inhibitor, that this molecule has an early protective effect after spinal cord contusion injury. Furthermore, wild-type mice treated for the first week after spinal cord contusion injury with recombinant secretory leukocyte protease inhibitor exhibit sustained improvement in locomotor control and reduced secondary tissue damage. Recombinant secretory leukocyte protease inhibitor injected intraperitoneally localizes to the nucleus of circulating leukocytes, is detected in the injured spinal cord, reduces activation of nuclear factor-κB and expression of tumour necrosis factor-α. Administration of recombinant secretory leukocyte protease inhibitor might therefore be useful for the treatment of acute spinal cord injury.

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Repertoire of microglial and macrophage responses after spinal cord injury

TL;DR: This work discusses the activation of macrophages and microglia following spinal cord injury, and their effects on repair, and suggests that harnessing their anti-inflammatory properties could pave the way for new therapeutic strategies for spinal cord trauma.
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From basics to clinical: a comprehensive review on spinal cord injury.

TL;DR: An extensive overview of SCI research, as well as its clinical component, is provided, covering areas from physiology and anatomy of the spinal cord, neuropathology of the SCI, current clinical options, neuronal plasticity after SCI and a variety of promising neuroprotective, cell-based and combinatorial therapeutic approaches that have recently moved, or are close to clinical testing.
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Macrophages: supportive cells for tissue repair and regeneration.

TL;DR: In the present review, few examples from various tissues are presented to illustrate that, beyond their specific properties in a given tissue, common features have been described that sustain a role of macrophages in the recovery and maintenance of tissue homeostasis.
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More friend than foe: the emerging role of neutrophils in tissue repair

TL;DR: The role of neutrophils in tissue damage and repair is scrutinized, discussing recent findings and raising unresolved questions around this intriguing immune cell.
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Macrophage polarization: a key event in the secondary phase of acute spinal cord injury

TL;DR: This review provides a comprehensive overview of the immuno‐pathophysiological features of acute SCI mainly from the following perspectives: the Overview of the pathophysiology of acuteSCI, the roles of macrophage, especially its polarization switch, and newly developed neuroprotective therapies modulating macrophages polarization in acute SCi.
References
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Journal ArticleDOI

Analysis of relative gene expression data using real-time quantitative pcr and the 2(-delta delta c(t)) method

TL;DR: The 2-Delta Delta C(T) method as mentioned in this paper was proposed to analyze the relative changes in gene expression from real-time quantitative PCR experiments, and it has been shown to be useful in the analysis of realtime, quantitative PCR data.
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Wound healing: an overview of acute, fibrotic and delayed healing.

TL;DR: This review describes the major biological processes associated with both normal and pathologic healing of acute wounds, characterized by four distinct, but overlapping phases: hemostasis, inflammation, proliferation and remodeling.
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Activation of interleukin-6 gene expression through the NF-kappa B transcription factor.

TL;DR: NF-kappa B is an important mediator for activation of the IL-6 gene by a variety of IL- 6 inducers in both U-937 and HeLa cells and that alternative inducible enhancer elements contribute in a cell-specific manner to IL-8 gene induction.
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Basso Mouse Scale for locomotion detects differences in recovery after spinal cord injury in five common mouse strains.

TL;DR: The differing behavioral response to SCI suggests inherent genetic factors significantly impact locomotor recovery and must be considered in studies with inbred or genetically engineered mouse strains.
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Rapid proteolysis of I kappa B-alpha is necessary for activation of transcription factor NF-kappa B.

TL;DR: It is reported that IκB-α (formerly MAD-3)11 is degraded in cells after stimulation with phorbol ester, interleukin-1, lipopolysaccharide and tumour necrosis factor-α, an event coincident with the appearance of active NF-κB.
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