Osteoblasts impair cholesterol synthesis in chondrocytes via Notch1 signalling.

Yueyi Yang, Demao Zhang, Daimo Guo, Jiachi Li, Siqun Xu, Jieya Wei, Jing Xie, Xuedong Zhou
Author Information
  1. Yueyi Yang: State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  2. Demao Zhang: State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  3. Daimo Guo: State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  4. Jiachi Li: State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  5. Siqun Xu: State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  6. Jieya Wei: State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
  7. Jing Xie: State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China. ORCID
  8. Xuedong Zhou: State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.

Abstract

OBJECTIVES: Previous reports have proposed the importance of signalling and material exchange between cartilage and subchondral bone. However, the specific experimental evidence is still insufficient to support the effect of this interdependent relationship on mutual cell behaviours. In this study, we aimed to investigate cellular lipid metabolism in chondrocytes induced by osteoblasts.
METHODS: Osteoblast-induced chondrocytes were established in a Transwell chamber. A cholesterol detection kit was used to detect cholesterol contents. RNA sequencing and qPCR were performed to assess changes in mRNA expression. Western blot analysis was performed to detect protein expression. Immunofluorescence staining was conducted to show the cellular distribution of proteins.
RESULTS: Cholesterol levels were significantly decreased in chondrocytes induced by osteoblasts. Osteoblasts reduced cholesterol synthesis in chondrocytes by reducing the expression of a series of synthetases, including Fdft1, Sqle, Lss, Cyp51, Msmo1, Nsdhl, Sc5d, Dhcr24 and Dhcr7. This modulatory process involves Notch1 signalling. The expression of ncstn and hey1, an activator and a specific downstream target of Notch signalling, respectively, were decreased in chondrocytes induced by osteoblasts.
CONCLUSIONS: For the first time, we elucidated that communication with osteoblasts reduces cholesterol synthesis in chondrocytes through Notch1 signalling. This result may provide a better understanding of the effect of subchondral bone signalling on chondrocytes.

Keywords

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Grants

  1. 81371136/National Natural Science Foundation of China
  2. 81430011/National Natural Science Foundation of China
  3. 81670978/National Natural Science Foundation of China
  4. 81771047/National Natural Science Foundation of China
  5. 81870754/National Natural Science Foundation of China

MeSH Term

Animals
Cholesterol
Chondrocytes
Mice
Osteoblasts
Receptor, Notch1
Signal Transduction

Chemicals

Notch1 protein, mouse
Receptor, Notch1
Cholesterol

Word Cloud

Created with Highcharts 10.0.0chondrocytescholesterolosteoblastssignallingexpressioninducedsynthesissubchondralbonespecificeffectcellulardetectperformeddecreasedOsteoblastsNotch1 signallingNotchOBJECTIVES:PreviousreportsproposedimportancematerialexchangecartilageHoweverexperimentalevidencestillinsufficientsupportinterdependentrelationshipmutualcellbehavioursstudyaimedinvestigatelipidmetabolismMETHODS:Osteoblast-inducedestablishedTranswellchamberdetectionkitusedcontentsRNAsequencingqPCRassesschangesmRNAWesternblotanalysisproteinImmunofluorescencestainingconductedshowdistributionproteinsRESULTS:CholesterollevelssignificantlyreducedreducingseriessynthetasesincludingFdft1SqleLssCyp51Msmo1NsdhlSc5dDhcr24Dhcr7modulatoryprocessinvolvesncstnhey1activatordownstreamtargetrespectivelyCONCLUSIONS:firsttimeelucidatedcommunicationreducesresultmayprovidebetterunderstandingimpairviaNotch1seladin-1

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