Schwann cells are the myelinating glial cells of the peripheral nervous system（PNS）.By establishing lipid-rich myelin sheaths around large-caliber axons,they ensure that electrical signal transmission is accelerated...Schwann cells are the myelinating glial cells of the peripheral nervous system（PNS）.By establishing lipid-rich myelin sheaths around large-caliber axons,they ensure that electrical signal transmission is accelerated-a process referred to as saltatory signal propagation.Apart from this prominent physiological function,these cells also exert important pathophysiological roles in PNS injuries or dis- eases. In contrast to the central nervous system （CNS）, the adult PNS retains a remarkably high degree of intrinsic re- generation. As a consequence, transected axons and dam- aged myelin sheaths can be repaired and nerve functional- ity can be restored. This spontaneous regenerative capacity depends on （inter） actions of macrophages, neurons, and Schwann cells.展开更多
Regeneration in the central nervous system （CNS） is limited, and CNS damage often leads to cognitive impairment or permanent functional motor and sensory loss. Impaired regenerative capacity is multifactorial and in...Regeneration in the central nervous system （CNS） is limited, and CNS damage often leads to cognitive impairment or permanent functional motor and sensory loss. Impaired regenerative capacity is multifactorial and includes inflammation, loss of the blood-brain barrier, and alteration in the extracellular matrix （ECM）. One of the main problems is the formation of a glial scar and the production of inhibitory ECM, such as proteoglycans, that generates a physical and mechanical barrier, impeding axonal regrowth （Figure 1A）.展开更多
Periodontal bone defects,primarily caused by periodontitis,are highly prevalent in clinical settings and manifest as bone fenestration,dehiscence,or attachment loss,presenting a significant challenge to oral health.In...Periodontal bone defects,primarily caused by periodontitis,are highly prevalent in clinical settings and manifest as bone fenestration,dehiscence,or attachment loss,presenting a significant challenge to oral health.In regenerative medicine,harnessing developmental principles for tissue repair offers promising therapeutic potential.Of particular interest is the condensation of progenitor cells,an essential event in organogenesis that has inspired clinically effective cell aggregation approaches in dental regeneration.However,the precise cellular coordination mechanisms during condensation and regeneration remain elusive.Here,taking the tooth as a model organ,we employed single-cell RNA sequencing to dissect the cellular composition and heterogeneity of human dental follicle and dental papilla,revealing a distinct Platelet-derived growth factor receptor alpha(PDGFRA)mesenchymal stem/stromal cell(MSC)population with remarkable odontogenic potential.Interestingly,a reciprocal paracrine interaction between PDGFRA^(+)dental follicle stem cells(DFSCs)and CD31^(+)Endomucin^(+)endothelial cells(ECs)was mediated by Vascular endothelial growth factor A(VEGFA)and Platelet-derived growth factor subunit BB(PDGFBB).This crosstalk not only maintains the functionality of PDGFRA^(+)DFSCs but also drives specialized angiogenesis.In vivo periodontal bone regeneration experiments further reveal that communication between PDGFRA+DFSC aggregates and recipient ECs is essential for effective angiogenic-osteogenic coupling and rapid tissue repair.Collectively,our results unravel the importance of MSC-EC crosstalk mediated by the VEGFA and PDGFBB-PDGFRA reciprocal signaling in orchestrating angiogenesis and osteogenesis.These findings not only establish a framework for deciphering and promoting periodontal bone regeneration in potential clinical applications but also offer insights for future therapeutic strategies in dental or broader regenerative medicine.展开更多
Human stem cells are scalable cell populations capable of cellular differentiation.This makes them a very attractive in vitro cellular resource and in theory provides unlimited amounts of primary cells.Such an approac...Human stem cells are scalable cell populations capable of cellular differentiation.This makes them a very attractive in vitro cellular resource and in theory provides unlimited amounts of primary cells.Such an approach has the potential to improve our understanding of human biology and treating disease.In the future it may be possible to deploy novel stem cell-based approaches to treat human liver diseases.In recent years,eff icient hepatic differentiation from human stem cells has been achieved by several research groups including our own.In this review we provide an overview of the f ield and discuss the future potential and limitations of stem cell technology.展开更多
基金supported by grants from the DFG(German Research Council)Novartis Pharma Gmb H(Nürnberg+2 种基金Germany)Baxter Innovations Gmb H(ViennaGermany)
文摘Schwann cells are the myelinating glial cells of the peripheral nervous system（PNS）.By establishing lipid-rich myelin sheaths around large-caliber axons,they ensure that electrical signal transmission is accelerated-a process referred to as saltatory signal propagation.Apart from this prominent physiological function,these cells also exert important pathophysiological roles in PNS injuries or dis- eases. In contrast to the central nervous system （CNS）, the adult PNS retains a remarkably high degree of intrinsic re- generation. As a consequence, transected axons and dam- aged myelin sheaths can be repaired and nerve functional- ity can be restored. This spontaneous regenerative capacity depends on （inter） actions of macrophages, neurons, and Schwann cells.
文摘Regeneration in the central nervous system （CNS） is limited, and CNS damage often leads to cognitive impairment or permanent functional motor and sensory loss. Impaired regenerative capacity is multifactorial and includes inflammation, loss of the blood-brain barrier, and alteration in the extracellular matrix （ECM）. One of the main problems is the formation of a glial scar and the production of inhibitory ECM, such as proteoglycans, that generates a physical and mechanical barrier, impeding axonal regrowth （Figure 1A）.
基金supported by grants from the National Key Research and Development Program of China(2022YFA1104400)the National Natural Science Foundation of China(82170988,82371020,82301028,82401201,82471011)+5 种基金the Young Science and Technology Rising Star Project of Shaanxi Province(2024ZC-KJXX-122)the China Postdoctoral Science Foundation(BX20230485)the Project of State Key Laboratory of Oral&Maxillofacial Reconstruction and Regeneration(2024MS04)the Shaanxi Provincial Health Research and Innovation Platform Construction Plan(2024PT-04)the“Rapid Response”Research projects(2023KXKT017 and 2023KXKT090)the Intramural Research Program project founded by Fourth Military Medical University(2024QMJJ008).
文摘Periodontal bone defects,primarily caused by periodontitis,are highly prevalent in clinical settings and manifest as bone fenestration,dehiscence,or attachment loss,presenting a significant challenge to oral health.In regenerative medicine,harnessing developmental principles for tissue repair offers promising therapeutic potential.Of particular interest is the condensation of progenitor cells,an essential event in organogenesis that has inspired clinically effective cell aggregation approaches in dental regeneration.However,the precise cellular coordination mechanisms during condensation and regeneration remain elusive.Here,taking the tooth as a model organ,we employed single-cell RNA sequencing to dissect the cellular composition and heterogeneity of human dental follicle and dental papilla,revealing a distinct Platelet-derived growth factor receptor alpha(PDGFRA)mesenchymal stem/stromal cell(MSC)population with remarkable odontogenic potential.Interestingly,a reciprocal paracrine interaction between PDGFRA^(+)dental follicle stem cells(DFSCs)and CD31^(+)Endomucin^(+)endothelial cells(ECs)was mediated by Vascular endothelial growth factor A(VEGFA)and Platelet-derived growth factor subunit BB(PDGFBB).This crosstalk not only maintains the functionality of PDGFRA^(+)DFSCs but also drives specialized angiogenesis.In vivo periodontal bone regeneration experiments further reveal that communication between PDGFRA+DFSC aggregates and recipient ECs is essential for effective angiogenic-osteogenic coupling and rapid tissue repair.Collectively,our results unravel the importance of MSC-EC crosstalk mediated by the VEGFA and PDGFBB-PDGFRA reciprocal signaling in orchestrating angiogenesis and osteogenesis.These findings not only establish a framework for deciphering and promoting periodontal bone regeneration in potential clinical applications but also offer insights for future therapeutic strategies in dental or broader regenerative medicine.
基金Supported by A RCUK fellowship,EP/E500145/1,to Hay DCA grant from the Edinburgh Bioquarter,to Medine CNChina Scholarship Council,No.2010658022,to Zhou WL
文摘Human stem cells are scalable cell populations capable of cellular differentiation.This makes them a very attractive in vitro cellular resource and in theory provides unlimited amounts of primary cells.Such an approach has the potential to improve our understanding of human biology and treating disease.In the future it may be possible to deploy novel stem cell-based approaches to treat human liver diseases.In recent years,eff icient hepatic differentiation from human stem cells has been achieved by several research groups including our own.In this review we provide an overview of the f ield and discuss the future potential and limitations of stem cell technology.
