000140045 001__ 140045 000140045 005__ 20240529143839.0 000140045 0247_ $$2doi$$a10.1172/JCI95305 000140045 0247_ $$2pmid$$apmid:29634489 000140045 0247_ $$2pmc$$apmc:PMC6025970 000140045 0247_ $$2ISSN$$a0021-9738 000140045 0247_ $$2ISSN$$a1558-8238 000140045 0247_ $$2altmetric$$aaltmetric:37241678 000140045 037__ $$aDZNE-2020-06367 000140045 041__ $$aEnglish 000140045 082__ $$a610 000140045 1001_ $$aKälin, Stefanie$$b0 000140045 245__ $$aCNS myeloid cells critically regulate heat hyperalgesia. 000140045 260__ $$aAnn Arbor, Mich.$$bASCJ$$c2018 000140045 264_1 $$2Crossref$$3online$$bAmerican Society for Clinical Investigation$$c2018-05-21 000140045 264_1 $$2Crossref$$3print$$bAmerican Society for Clinical Investigation$$c2018-07-02 000140045 3367_ $$2DRIVER$$aarticle 000140045 3367_ $$2DataCite$$aOutput Types/Journal article 000140045 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1714744039_29 000140045 3367_ $$2BibTeX$$aARTICLE 000140045 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000140045 3367_ $$00$$2EndNote$$aJournal Article 000140045 520__ $$aActivation of non-neuronal microglia is thought to play a causal role in spinal processing of neuropathic pain. To specifically investigate microglia-mediated effects in a model of neuropathic pain and overcome the methodological limitations of previous approaches exploring microglia function upon nerve injury, we selectively ablated resident microglia by intracerebroventricular ganciclovir infusion into male CD11b-HSVTK-transgenic mice, which was followed by a rapid, complete, and persistent (23 weeks) repopulation of the CNS by peripheral myeloid cells. In repopulated mice that underwent sciatic nerve injury, we observed a normal response to mechanical stimuli, but an absence of thermal hypersensitivity ipsilateral to the injured nerve. Furthermore, we found that neuronal expression of calcitonin gene-related peptide (CGRP), which is a marker of neurons essential for heat responses, was diminished in the dorsal horn of the spinal cord in repopulated mice. These findings identify distinct mechanisms for heat and mechanical hypersensitivity and highlight a crucial contribution of CNS myeloid cells in the facilitation of noxious heat. 000140045 536__ $$0G:(DE-HGF)POF3-342$$a342 - Disease Mechanisms and Model Systems (POF3-342)$$cPOF3-342$$fPOF III$$x0 000140045 588__ $$aDataset connected to CrossRef, PubMed, 000140045 650_7 $$2NLM Chemicals$$aPeptide Fragments 000140045 650_7 $$2NLM Chemicals$$acalcitonin gene related peptide (1-7) 000140045 650_7 $$0JHB2QIZ69Z$$2NLM Chemicals$$aCalcitonin Gene-Related Peptide 000140045 650_2 $$2MeSH$$aAnimals 000140045 650_2 $$2MeSH$$aCalcitonin Gene-Related Peptide: physiology 000140045 650_2 $$2MeSH$$aCentral Nervous System: pathology 000140045 650_2 $$2MeSH$$aCentral Nervous System: physiopathology 000140045 650_2 $$2MeSH$$aHot Temperature 000140045 650_2 $$2MeSH$$aHyperalgesia: pathology 000140045 650_2 $$2MeSH$$aHyperalgesia: physiopathology 000140045 650_2 $$2MeSH$$aMale 000140045 650_2 $$2MeSH$$aMice 000140045 650_2 $$2MeSH$$aMice, Inbred C57BL 000140045 650_2 $$2MeSH$$aMice, Transgenic 000140045 650_2 $$2MeSH$$aMicroglia: cytology 000140045 650_2 $$2MeSH$$aMicroglia: physiology 000140045 650_2 $$2MeSH$$aMyeloid Cells: pathology 000140045 650_2 $$2MeSH$$aMyeloid Cells: physiology 000140045 650_2 $$2MeSH$$aNeuralgia: pathology 000140045 650_2 $$2MeSH$$aNeuralgia: physiopathology 000140045 650_2 $$2MeSH$$aPeptide Fragments: physiology 000140045 650_2 $$2MeSH$$aPeripheral Nerve Injuries: pathology 000140045 650_2 $$2MeSH$$aPeripheral Nerve Injuries: physiopathology 000140045 650_2 $$2MeSH$$aPeripheral Nerves: pathology 000140045 650_2 $$2MeSH$$aPeripheral Nerves: physiopathology 000140045 650_2 $$2MeSH$$aSpinal Cord Dorsal Horn: pathology 000140045 650_2 $$2MeSH$$aSpinal Cord Dorsal Horn: physiopathology 000140045 7001_ $$aMiller, Kelly R$$b1 000140045 7001_ $$aKälin, Roland E$$b2 000140045 7001_ $$aJendrach, Marina$$b3 000140045 7001_ $$aWitzel, Christian$$b4 000140045 7001_ $$0P:(DE-2719)2812386$$aHeppner, Frank L$$b5$$eLast author$$udzne 000140045 77318 $$2Crossref$$3journal-article$$a10.1172/jci95305$$b : American Society for Clinical Investigation, 2018-05-21$$n7$$p2774-2786$$tJournal of Clinical Investigation$$v128$$x0021-9738$$y2018 000140045 773__ $$0PERI:(DE-600)2018375-6$$a10.1172/JCI95305$$gVol. 128, no. 7, p. 2774 - 2786$$n7$$p2774-2786$$q128:7<2774 - 2786$$tThe journal of clinical investigation$$v128$$x0021-9738$$y2018 000140045 8567_ $$2Pubmed Central$$uhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025970 000140045 8564_ $$uhttps://pub.dzne.de/record/140045/files/DZNE-2020-06367_Restricted.pdf 000140045 8564_ $$uhttps://pub.dzne.de/record/140045/files/DZNE-2020-06367_Restricted.pdf?subformat=pdfa$$xpdfa 000140045 909CO $$ooai:pub.dzne.de:140045$$pVDB$$qdnbdelivery 000140045 9101_ $$0I:(DE-588)1065079516$$6P:(DE-2719)2812386$$aDeutsches Zentrum für Neurodegenerative Erkrankungen$$b5$$kDZNE 000140045 9131_ 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