Wen Xing, Fang Dong, Yining Liu, Jiajia Yuan, Chao Chen, Yihan Li, Han Wang, Ming Yao, Ting Chen, Tao Cheng, Sha Hao, Yuan Zhou
{"title":"p18INK4c的缺失增强了骨髓间充质基质细胞的成骨和造血支持能力。","authors":"Wen Xing, Fang Dong, Yining Liu, Jiajia Yuan, Chao Chen, Yihan Li, Han Wang, Ming Yao, Ting Chen, Tao Cheng, Sha Hao, Yuan Zhou","doi":"10.1186/s13287-025-04402-6","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>p18<sup>INK4 C</sup> (CDKN2C, encoded by p18<sup>INK4c</sup> or Cdkn2c) is an early G1-phase cyclin-dependent kinase inhibitor protein. Previous studies demonstrated enhanced self-renewal capacity of hematopoietic stem cells (HSCs) in p18<sup>-/-</sup> mice compared to wild-type (WT) mice. Given the critical role of bone marrow niche cells-particularly mesenchymal stromal cells (MSCs)-in hematopoiesis, this study investigated the functional alterations of p18<sup>-/-</sup> MSCs and their impact on hematopoietic support.</p><p><strong>Methods: </strong>Bone marrow derived MSCs were isolated from p18<sup>-/-</sup> and WT mice. Their proliferation and differentiation capacities were assessed, followed by evaluation of hematopoietic support using cobblestone area-forming cell assay and long-term culture-initiating cell assay. RNA sequencing was performed to analyze the transcriptional profile of p18<sup>-/-</sup> MSCs, with a focus on differentially expressed genes (DEGs). Key pathways associated with hematopoietic support were identified using Ingenuity Pathway Analysis. A candidate protein was quantified by ELISA, and its functional role in hematopoietic support was validated via a modified coculture system.</p><p><strong>Results: </strong>p18<sup>-/-</sup> MSCs displayed an increased proliferation rate, preferential differentiation toward osteogenesis over adipogenesis, and enhanced hematopoietic support. RNA sequencing analysis identified 137 DEGs, with secreted phosphoprotein 1 (Spp1, encoding osteopontin, Opn) being significantly upregulated in p18<sup>-/-</sup> MSCs. Elevated Opn levels were confirmed in both bone marrow and MSC-conditioned media from p18<sup>-/-</sup> mice. Functional validation further demonstrated that Opn enhanced the hematopoietic supportive capacity of MSCs in vitro.</p><p><strong>Conclusions: </strong>p18 deficiency promotes osteogenic differentiation and enhances the hematopoietic supportive function of MSCs, likely mediated by Opn upregulation. These findings suggest a potential therapeutic strategy for improving bone regeneration and HSC expansion.</p>","PeriodicalId":21876,"journal":{"name":"Stem Cell Research & Therapy","volume":"16 1","pages":"334"},"PeriodicalIF":7.1000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12210517/pdf/","citationCount":"0","resultStr":"{\"title\":\"Deletion of p18<sup>INK4c</sup> enhances both osteogenesis and hematopoietic supportive capacity of bone marrow mesenchymal stromal cells.\",\"authors\":\"Wen Xing, Fang Dong, Yining Liu, Jiajia Yuan, Chao Chen, Yihan Li, Han Wang, Ming Yao, Ting Chen, Tao Cheng, Sha Hao, Yuan Zhou\",\"doi\":\"10.1186/s13287-025-04402-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>p18<sup>INK4 C</sup> (CDKN2C, encoded by p18<sup>INK4c</sup> or Cdkn2c) is an early G1-phase cyclin-dependent kinase inhibitor protein. Previous studies demonstrated enhanced self-renewal capacity of hematopoietic stem cells (HSCs) in p18<sup>-/-</sup> mice compared to wild-type (WT) mice. Given the critical role of bone marrow niche cells-particularly mesenchymal stromal cells (MSCs)-in hematopoiesis, this study investigated the functional alterations of p18<sup>-/-</sup> MSCs and their impact on hematopoietic support.</p><p><strong>Methods: </strong>Bone marrow derived MSCs were isolated from p18<sup>-/-</sup> and WT mice. Their proliferation and differentiation capacities were assessed, followed by evaluation of hematopoietic support using cobblestone area-forming cell assay and long-term culture-initiating cell assay. RNA sequencing was performed to analyze the transcriptional profile of p18<sup>-/-</sup> MSCs, with a focus on differentially expressed genes (DEGs). Key pathways associated with hematopoietic support were identified using Ingenuity Pathway Analysis. A candidate protein was quantified by ELISA, and its functional role in hematopoietic support was validated via a modified coculture system.</p><p><strong>Results: </strong>p18<sup>-/-</sup> MSCs displayed an increased proliferation rate, preferential differentiation toward osteogenesis over adipogenesis, and enhanced hematopoietic support. RNA sequencing analysis identified 137 DEGs, with secreted phosphoprotein 1 (Spp1, encoding osteopontin, Opn) being significantly upregulated in p18<sup>-/-</sup> MSCs. Elevated Opn levels were confirmed in both bone marrow and MSC-conditioned media from p18<sup>-/-</sup> mice. Functional validation further demonstrated that Opn enhanced the hematopoietic supportive capacity of MSCs in vitro.</p><p><strong>Conclusions: </strong>p18 deficiency promotes osteogenic differentiation and enhances the hematopoietic supportive function of MSCs, likely mediated by Opn upregulation. These findings suggest a potential therapeutic strategy for improving bone regeneration and HSC expansion.</p>\",\"PeriodicalId\":21876,\"journal\":{\"name\":\"Stem Cell Research & Therapy\",\"volume\":\"16 1\",\"pages\":\"334\"},\"PeriodicalIF\":7.1000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12210517/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Stem Cell Research & Therapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s13287-025-04402-6\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CELL & TISSUE ENGINEERING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem Cell Research & Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13287-025-04402-6","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL & TISSUE ENGINEERING","Score":null,"Total":0}
Deletion of p18INK4c enhances both osteogenesis and hematopoietic supportive capacity of bone marrow mesenchymal stromal cells.
Background: p18INK4 C (CDKN2C, encoded by p18INK4c or Cdkn2c) is an early G1-phase cyclin-dependent kinase inhibitor protein. Previous studies demonstrated enhanced self-renewal capacity of hematopoietic stem cells (HSCs) in p18-/- mice compared to wild-type (WT) mice. Given the critical role of bone marrow niche cells-particularly mesenchymal stromal cells (MSCs)-in hematopoiesis, this study investigated the functional alterations of p18-/- MSCs and their impact on hematopoietic support.
Methods: Bone marrow derived MSCs were isolated from p18-/- and WT mice. Their proliferation and differentiation capacities were assessed, followed by evaluation of hematopoietic support using cobblestone area-forming cell assay and long-term culture-initiating cell assay. RNA sequencing was performed to analyze the transcriptional profile of p18-/- MSCs, with a focus on differentially expressed genes (DEGs). Key pathways associated with hematopoietic support were identified using Ingenuity Pathway Analysis. A candidate protein was quantified by ELISA, and its functional role in hematopoietic support was validated via a modified coculture system.
Results: p18-/- MSCs displayed an increased proliferation rate, preferential differentiation toward osteogenesis over adipogenesis, and enhanced hematopoietic support. RNA sequencing analysis identified 137 DEGs, with secreted phosphoprotein 1 (Spp1, encoding osteopontin, Opn) being significantly upregulated in p18-/- MSCs. Elevated Opn levels were confirmed in both bone marrow and MSC-conditioned media from p18-/- mice. Functional validation further demonstrated that Opn enhanced the hematopoietic supportive capacity of MSCs in vitro.
Conclusions: p18 deficiency promotes osteogenic differentiation and enhances the hematopoietic supportive function of MSCs, likely mediated by Opn upregulation. These findings suggest a potential therapeutic strategy for improving bone regeneration and HSC expansion.
期刊介绍:
Stem Cell Research & Therapy serves as a leading platform for translational research in stem cell therapies. This international, peer-reviewed journal publishes high-quality open-access research articles, with a focus on basic, translational, and clinical research in stem cell therapeutics and regenerative therapies. Coverage includes animal models and clinical trials. Additionally, the journal offers reviews, viewpoints, commentaries, and reports.