Single nuclear‐spatial transcriptomic sequencing reveals distinct puncture‐induced cell subpopulations in the intervertebral disc of a rat model
Abstract Objective We aim to investigate the spatiotemporal dynamics of intervertebral disc (IVD) cell subpopulations in IVD degeneration (IVDD). Methods To gain combined spatial and transcriptomic insights into IVDD, we employed both spatial transcriptomic sequencing (stRNA‐seq) and single nucleus...
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Wiley
2025-06-01
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| Series: | Clinical and Translational Medicine |
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| Online Access: | https://doi.org/10.1002/ctm2.70370 |
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| author | Guoyan Liang Jing Tan Chong Chen Yuying Liu Yongyu Ye Xiaolin Pan Qiujian Zheng Yunbing Chang Feng‐Juan Lyu |
| author_facet | Guoyan Liang Jing Tan Chong Chen Yuying Liu Yongyu Ye Xiaolin Pan Qiujian Zheng Yunbing Chang Feng‐Juan Lyu |
| author_sort | Guoyan Liang |
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| description | Abstract Objective We aim to investigate the spatiotemporal dynamics of intervertebral disc (IVD) cell subpopulations in IVD degeneration (IVDD). Methods To gain combined spatial and transcriptomic insights into IVDD, we employed both spatial transcriptomic sequencing (stRNA‐seq) and single nucleus RNA sequencing (snRNA‐seq) in a rat puncture‐induced IVDD model. The findings were verified in rat and human IVD by immunostaining and qRT‐PCR. Tamoxifen‐administered PdgfraCreERT2;R26tdTomato mice were adopted to track platelet‐derived growth factor receptor alpha (Pdgfra) positive cells. Results Puncture response regions were revealed on day 1 post‐puncture, for which oxidative stress emerged as a prominent pathway in a Stress Zone consisting of lipocalin‐2 (Lcn2)+ annulus fibrosus (AF) cells (AFC), which propagated and migrated into nucleus pulposus (NP), playing a key role in delivering injury signals and triggering pathological processes, including ferroptosis, fibrosis, and immune reactions. In the NP, Collagen 3‐high (Col3hi) NP cells (NPC) were another induced population demonstrating a fibrochondrocyte‐like phenotype and high epithelial–mesenchymal transition activation, an important pathway involved in tissue fibrosis. Crucially, lineage tracing experiments in PdgfraCreERT2;R26tdTomat mice revealed the significant migration and proliferation of Pdgfra+ AFCs from the AF into the NP following puncture. These findings provide direct evidence that both Pdgfra+ AFCs and Col3hi NP cells may contribute to NP fibrosis. Conclusion Puncture‐induced oxidative stress in a stress zone is the primary reaction playing an important role in initiating IVDD. Several puncture‐induced cell subpopulations were identified, including Lcn2+ AFC, Col3hi NPC, and Pdgfra+ AFC. Lcn2+ AFC plays a pivotal role in connecting oxidative stress with other pathological processes. Our results clarified the dual origin of Pdgfra+ cells, highlighting the contribution of AF‐derived cells to the NP during degeneration and emphasizing the complexity of cellular changes underlying NP fibrosis. Further investigation into the specific contributions of Pdgfra+ cells from different origins to fibrosis is warranted. Key points Puncture induced oxidative stress in a Stress Zone is the primary reaction in initiating IVDD. Puncture induced several IVD cell subpopulations, including Lcn2+ AFC, Col3hi NPC and Pdgfra+ AFC. Lcn2+ AFC plays a pivotal role in connecting oxidative stress with other pathological processes. Pdgfra+ cells in the NP derived from both Pdgfra+ AFC and Col3hi NPC, highlighting dual origin of NP fibrosis. |
| format | Article |
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| institution | Kabale University |
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| language | English |
| publishDate | 2025-06-01 |
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| spelling | doaj-art-8d5f48b6fb9f42d5871272d421ec664e2025-08-20T03:32:15ZengWileyClinical and Translational Medicine2001-13262025-06-01156n/an/a10.1002/ctm2.70370Single nuclear‐spatial transcriptomic sequencing reveals distinct puncture‐induced cell subpopulations in the intervertebral disc of a rat modelGuoyan Liang0Jing Tan1Chong Chen2Yuying Liu3Yongyu Ye4Xiaolin Pan5Qiujian Zheng6Yunbing Chang7Feng‐Juan Lyu8Department of Spine Surgery Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences) Southern Medical University Guangzhou P.R. ChinaSchool of Medicine Joint Center for Regenerative Medicine Research of South China University of Technology and the University of Western Australia South China University of Technology Guangzhou P.R. ChinaDepartment of Spine Surgery Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences) Southern Medical University Guangzhou P.R. ChinaSchool of Medicine Joint Center for Regenerative Medicine Research of South China University of Technology and the University of Western Australia South China University of Technology Guangzhou P.R. ChinaDepartment of Spine Surgery Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences) Southern Medical University Guangzhou P.R. ChinaSchool of Medicine Joint Center for Regenerative Medicine Research of South China University of Technology and the University of Western Australia South China University of Technology Guangzhou P.R. ChinaDepartment of Trauma Surgery & Joint Surgery Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences) Southern Medical University Guangzhou P.R. ChinaDepartment of Spine Surgery Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences) Southern Medical University Guangzhou P.R. ChinaSchool of Medicine South China University of Technology Guangzhou P.R. ChinaAbstract Objective We aim to investigate the spatiotemporal dynamics of intervertebral disc (IVD) cell subpopulations in IVD degeneration (IVDD). Methods To gain combined spatial and transcriptomic insights into IVDD, we employed both spatial transcriptomic sequencing (stRNA‐seq) and single nucleus RNA sequencing (snRNA‐seq) in a rat puncture‐induced IVDD model. The findings were verified in rat and human IVD by immunostaining and qRT‐PCR. Tamoxifen‐administered PdgfraCreERT2;R26tdTomato mice were adopted to track platelet‐derived growth factor receptor alpha (Pdgfra) positive cells. Results Puncture response regions were revealed on day 1 post‐puncture, for which oxidative stress emerged as a prominent pathway in a Stress Zone consisting of lipocalin‐2 (Lcn2)+ annulus fibrosus (AF) cells (AFC), which propagated and migrated into nucleus pulposus (NP), playing a key role in delivering injury signals and triggering pathological processes, including ferroptosis, fibrosis, and immune reactions. In the NP, Collagen 3‐high (Col3hi) NP cells (NPC) were another induced population demonstrating a fibrochondrocyte‐like phenotype and high epithelial–mesenchymal transition activation, an important pathway involved in tissue fibrosis. Crucially, lineage tracing experiments in PdgfraCreERT2;R26tdTomat mice revealed the significant migration and proliferation of Pdgfra+ AFCs from the AF into the NP following puncture. These findings provide direct evidence that both Pdgfra+ AFCs and Col3hi NP cells may contribute to NP fibrosis. Conclusion Puncture‐induced oxidative stress in a stress zone is the primary reaction playing an important role in initiating IVDD. Several puncture‐induced cell subpopulations were identified, including Lcn2+ AFC, Col3hi NPC, and Pdgfra+ AFC. Lcn2+ AFC plays a pivotal role in connecting oxidative stress with other pathological processes. Our results clarified the dual origin of Pdgfra+ cells, highlighting the contribution of AF‐derived cells to the NP during degeneration and emphasizing the complexity of cellular changes underlying NP fibrosis. Further investigation into the specific contributions of Pdgfra+ cells from different origins to fibrosis is warranted. Key points Puncture induced oxidative stress in a Stress Zone is the primary reaction in initiating IVDD. Puncture induced several IVD cell subpopulations, including Lcn2+ AFC, Col3hi NPC and Pdgfra+ AFC. Lcn2+ AFC plays a pivotal role in connecting oxidative stress with other pathological processes. Pdgfra+ cells in the NP derived from both Pdgfra+ AFC and Col3hi NPC, highlighting dual origin of NP fibrosis.https://doi.org/10.1002/ctm2.70370intervertebral disc degenerationLCN2oxidative stressPDGFRAsingle‐nucleus RNA sequencingspatial transcriptomic |
| spellingShingle | Guoyan Liang Jing Tan Chong Chen Yuying Liu Yongyu Ye Xiaolin Pan Qiujian Zheng Yunbing Chang Feng‐Juan Lyu Single nuclear‐spatial transcriptomic sequencing reveals distinct puncture‐induced cell subpopulations in the intervertebral disc of a rat model Clinical and Translational Medicine intervertebral disc degeneration LCN2 oxidative stress PDGFRA single‐nucleus RNA sequencing spatial transcriptomic |
| title | Single nuclear‐spatial transcriptomic sequencing reveals distinct puncture‐induced cell subpopulations in the intervertebral disc of a rat model |
| title_full | Single nuclear‐spatial transcriptomic sequencing reveals distinct puncture‐induced cell subpopulations in the intervertebral disc of a rat model |
| title_fullStr | Single nuclear‐spatial transcriptomic sequencing reveals distinct puncture‐induced cell subpopulations in the intervertebral disc of a rat model |
| title_full_unstemmed | Single nuclear‐spatial transcriptomic sequencing reveals distinct puncture‐induced cell subpopulations in the intervertebral disc of a rat model |
| title_short | Single nuclear‐spatial transcriptomic sequencing reveals distinct puncture‐induced cell subpopulations in the intervertebral disc of a rat model |
| title_sort | single nuclear spatial transcriptomic sequencing reveals distinct puncture induced cell subpopulations in the intervertebral disc of a rat model |
| topic | intervertebral disc degeneration LCN2 oxidative stress PDGFRA single‐nucleus RNA sequencing spatial transcriptomic |
| url | https://doi.org/10.1002/ctm2.70370 |
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