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Regulatory mechanism of CCN2 production by serotonin (5-HT) via 5-HT(2A) and 5-HT(2B) receptors in chondrocytes

Serotonin (5-hydroxytryptamine: 5-HT) is recognized as a neurotransmitter in the central nerve system and as a regulator of systemic blood pressure in the peripheral tissues. Recently, it was reported that 5-HT(2) receptors (5-HT(2)Rs) were expressed in cartilage tissues lacking both vessels and neu...

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Detalles Bibliográficos
Autores principales: Hori, Ayaka, Nishida, Takashi, Takashiba, Shogo, Kubota, Satoshi, Takigawa, Masaharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690650/
https://www.ncbi.nlm.nih.gov/pubmed/29145495
http://dx.doi.org/10.1371/journal.pone.0188014
Descripción
Sumario:Serotonin (5-hydroxytryptamine: 5-HT) is recognized as a neurotransmitter in the central nerve system and as a regulator of systemic blood pressure in the peripheral tissues. Recently, it was reported that 5-HT(2) receptors (5-HT(2)Rs) were expressed in cartilage tissues lacking both vessels and neurons, suggesting possible novel functions of 5-HT during cartilage development and regeneration. Our previous data indicated that CCN family protein 2/connective tissue growth factor (CCN2/CTGF) plays a central role in cartilage development and regeneration. Therefore, the aim of this study was to investigate the effect of 5-HT on the production of CCN2 in chondrocytes. Firstly, we showed that the mRNAs of 5-HT(2)R subtypes 5-HT(2A)R and 5-HT(2B)R, were expressed in a human chondrocytic cell line, HCS-2/8; however, 5-HT(2C)R mRNA was not detected. In addition, exogenously added 5-HT did not affect the 5-HT(2A)R and 5-HT(2B)R expressions. Next, we demonstrated that CCN2 production was increased by treatment with a 5-HT(2A)R agonist and the combination of 5-HT and 5-HT(2B)R antagonist. In contrast, treatment with a 5-HT(2B)R agonist and the combination of 5-HT and 5-HT(2A)R antagonist decreased CCN2 production. Furthermore, we showed that phosphorylation of Akt and p38 MAPK were increased by treatment with 5-HT(2A)R agonist, and that phosphorylation of PKCε, PKCζ, ERK1/2 and JNK were increased by treatment with 5-HT(2B)R agonist. Finally, we found that 5-HT(2A)R was localized in the growth plate, whereas 5-HT(2B)R was localized in the articular cartilage. These findings suggest that 5-HT promotes CCN2 production through the 5-HT(2A)R in growth plates, and that it represses CCN2 production through the 5-HT(2B)R in articular cartilage for harmonized development of long bones.