Circadian regulation of chemotherapy-induced peripheral neuropathic pain and the underlying transcriptomic landscape
Autor: | Kazuhiro Yagita, Mark J. Burish, Jin Mo Chung, Nobuya Koike, Marvin Wirianto, Hee Kee Kim, Sun Yeul Lee, Zheng Chen, Salahadin Abdi, Hyun Kyoung Lee, Eunju Kim, Seung Hee Yoo |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Spinal Cord Dorsal Horn medicine.medical_specialty Paclitaxel Neurophysiology Gene Expression lcsh:Medicine In Vitro Techniques Biology Article Mice 03 medical and health sciences 0302 clinical medicine Peripheral Nerve Injuries Ganglia Spinal Internal medicine medicine Zeitgeber Animals Circadian rhythm lcsh:Science Multidisciplinary lcsh:R ARNTL Transcription Factors Period Circadian Proteins Antineoplastic Agents Phytogenic Circadian Rhythm Rats PER2 CLOCK Disease Models Animal 030104 developmental biology Endocrinology Allodynia Neuropathic pain Peripheral nerve injury Neuralgia lcsh:Q Circadian rhythms and sleep medicine.symptom 030217 neurology & neurosurgery |
Zdroj: | Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-020-70757-w |
Popis: | Growing evidence demonstrates circadian rhythms of pain hypersensitivity in various chronic disorders. In chemotherapy-induced peripheral neuropathy (CIPN), agents such as paclitaxel are known to elicit chronic neuropathic pain in cancer patients and seriously compromise their quality of life. Here, we report that the mechanical threshold for allodynia in paclitaxel-treated rats exhibited a robust circadian oscillation, reaching the nadir during the daytime (inactive phase). Using Per2::LucSV circadian reporter mice expressing a PER2::LUC fusion protein, we isolated dorsal root ganglia (DRG), the primary sensory cell body for peripheral nerve injury generated hypersensitivity, and monitored ex vivo reporter bioluminescence. We observed strong circadian reporter rhythms in DRG neurons which are highly entrainable by external cues. Paclitaxel treatment significantly lengthened DRG circadian periods, with little effects on the amplitude of oscillation. We further observed the core protein BMAL1 and PER2 in DRG neurons and satellite cells. Using DRG and dorsal horn (DH; another key structure for CIPN pain response) tissues from vehicle and paclitaxel treated rats, we performed RNA-sequencing and identified diurnal expression of core clock genes as well as clock-controlled genes in both sites. Interestingly, 20.1% and 30.4% of diurnal differentially expressed genes (DEGs) overlapped with paclitaxel-induced DEGs in the DRG and the DH respectively. In contrast, paclitaxel-induced DEGs displayed only a modest overlap between daytime and nighttime (Zeitgeber Time 8 and 20). Furthermore, paclitaxel treatment induced de novo diurnal DEGs, suggesting reciprocal interaction of circadian rhythms and chemotherapy. Our study therefore demonstrates a circadian oscillation of CIPN and its underlying transcriptomic landscape. |
Databáze: | OpenAIRE |
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