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In vivo immune interactions of multipotent stromal cells underlie their long-lasting pain-relieving effect
by
Jia-Le Yang
, Wei Guo
, Huakun Xu
, Satoshi Imai
, Yu-Xia Chu
, Zaid Mohammad
, Kamal D. Moudgil
, Mineo Watanabe
, Shiping Zou
, Ronald Dubner
, Feng Wei
, Ke Ren
in
13/100
/ 13/21
/ 13/51
/ 13/89
/ 14/105
/ 14/63
/ 631/378/371
/ 64/110
/ 64/60
/ 692/308/2778
/ Animals
/ Bone marrow
/ CC chemokine receptors
/ CCR2 protein
/ Cell activation
/ Chemokine CCL4
/ Chemokine CXCL1
/ Chemokines
/ Chemotactic factors
/ CXCR2 protein
/ Cytokines
/ Dentistry
/ Female
/ Gene expression
/ Humanities and Social Sciences
/ Hyperalgesia
/ Immune system
/ Immunomodulation
/ Immunoregulation
/ Intravenous administration
/ Ligands
/ Macrophages
/ Male
/ Mesenchymal Stem Cells
/ Monocyte chemoattractant protein 1
/ Monocytes
/ multidisciplinary
/ Narcotics
/ Neurosciences
/ Opioid receptors (type mu)
/ Pain
/ Rats
/ Rats, Sprague-Dawley
/ Receptors, CCR2
/ Receptors, Opioid, mu
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Stromal cells
2017
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In vivo immune interactions of multipotent stromal cells underlie their long-lasting pain-relieving effect
by
Jia-Le Yang
, Wei Guo
, Huakun Xu
, Satoshi Imai
, Yu-Xia Chu
, Zaid Mohammad
, Kamal D. Moudgil
, Mineo Watanabe
, Shiping Zou
, Ronald Dubner
, Feng Wei
, Ke Ren
in
13/100
/ 13/21
/ 13/51
/ 13/89
/ 14/105
/ 14/63
/ 631/378/371
/ 64/110
/ 64/60
/ 692/308/2778
/ Animals
/ Bone marrow
/ CC chemokine receptors
/ CCR2 protein
/ Cell activation
/ Chemokine CCL4
/ Chemokine CXCL1
/ Chemokines
/ Chemotactic factors
/ CXCR2 protein
/ Cytokines
/ Dentistry
/ Female
/ Gene expression
/ Humanities and Social Sciences
/ Hyperalgesia
/ Immune system
/ Immunomodulation
/ Immunoregulation
/ Intravenous administration
/ Ligands
/ Macrophages
/ Male
/ Mesenchymal Stem Cells
/ Monocyte chemoattractant protein 1
/ Monocytes
/ multidisciplinary
/ Narcotics
/ Neurosciences
/ Opioid receptors (type mu)
/ Pain
/ Rats
/ Rats, Sprague-Dawley
/ Receptors, CCR2
/ Receptors, Opioid, mu
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Stromal cells
2017
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In vivo immune interactions of multipotent stromal cells underlie their long-lasting pain-relieving effect
by
Jia-Le Yang
, Wei Guo
, Huakun Xu
, Satoshi Imai
, Yu-Xia Chu
, Zaid Mohammad
, Kamal D. Moudgil
, Mineo Watanabe
, Shiping Zou
, Ronald Dubner
, Feng Wei
, Ke Ren
in
13/100
/ 13/21
/ 13/51
/ 13/89
/ 14/105
/ 14/63
/ 631/378/371
/ 64/110
/ 64/60
/ 692/308/2778
/ Animals
/ Bone marrow
/ CC chemokine receptors
/ CCR2 protein
/ Cell activation
/ Chemokine CCL4
/ Chemokine CXCL1
/ Chemokines
/ Chemotactic factors
/ CXCR2 protein
/ Cytokines
/ Dentistry
/ Female
/ Gene expression
/ Humanities and Social Sciences
/ Hyperalgesia
/ Immune system
/ Immunomodulation
/ Immunoregulation
/ Intravenous administration
/ Ligands
/ Macrophages
/ Male
/ Mesenchymal Stem Cells
/ Monocyte chemoattractant protein 1
/ Monocytes
/ multidisciplinary
/ Narcotics
/ Neurosciences
/ Opioid receptors (type mu)
/ Pain
/ Rats
/ Rats, Sprague-Dawley
/ Receptors, CCR2
/ Receptors, Opioid, mu
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Stromal cells
2017
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In vivo immune interactions of multipotent stromal cells underlie their long-lasting pain-relieving effect
Journal Article
In vivo immune interactions of multipotent stromal cells underlie their long-lasting pain-relieving effect
2017
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Overview
Systemic infusion of bone marrow stromal cells (BMSCs), a major type of multipotent stromal cells, produces pain relief (antihyperalgesia) that lasts for months. However, studies have shown that the majority of BMSCs are trapped in the lungs immediately after intravenous infusion and their survival time in the host is inconsistent with their lengthy antihyperalgesia. Here we show that long-lasting antihyperalgesia produced by BMSCs required their chemotactic factors such as CCL4 and CCR2, the integrations with the monocytes/macrophages population, and BMSC-induced monocyte CXCL1. The activation of central mu-opioid receptors related to CXCL1-CXCR2 signaling plays an important role in BMSC-produced antihyperalgesia. Our findings suggest that the maintenance of antihypergesia can be achieved by immune regulation without actual engraftment of BMSCs. In the capacity of therapeutic use of BMSCs other than structural repair and replacement, more attention should be directed to their role as immune modulators and subsequent alterations in the immune system.
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