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1.
Nature ; 513(7519): 551-4, 2014 Sep 25.
Artigo em Inglês | MEDLINE | ID: mdl-25079316

RESUMO

Mesenchymal stem cells occupy niches in stromal tissues where they provide sources of cells for specialized mesenchymal derivatives during growth and repair. The origins of mesenchymal stem cells have been the subject of considerable discussion, and current consensus holds that perivascular cells form mesenchymal stem cells in most tissues. The continuously growing mouse incisor tooth offers an excellent model to address the origin of mesenchymal stem cells. These stem cells dwell in a niche at the tooth apex where they produce a variety of differentiated derivatives. Cells constituting the tooth are mostly derived from two embryonic sources: neural crest ectomesenchyme and ectodermal epithelium. It has been thought for decades that the dental mesenchymal stem cells giving rise to pulp cells and odontoblasts derive from neural crest cells after their migration in the early head and formation of ectomesenchymal tissue. Here we show that a significant population of mesenchymal stem cells during development, self-renewal and repair of a tooth are derived from peripheral nerve-associated glia. Glial cells generate multipotent mesenchymal stem cells that produce pulp cells and odontoblasts. By combining a clonal colour-coding technique with tracing of peripheral glia, we provide new insights into the dynamics of tooth organogenesis and growth.


Assuntos
Diferenciação Celular , Linhagem da Célula , Incisivo/citologia , Células-Tronco Mesenquimais/citologia , Neuroglia/citologia , Animais , Rastreamento de Células , Células Clonais/citologia , Polpa Dentária/citologia , Feminino , Incisivo/embriologia , Masculino , Camundongos , Modelos Biológicos , Crista Neural/citologia , Odontoblastos/citologia , Regeneração , Células de Schwann/citologia
2.
Science ; 345(6192): 82-7, 2014 Jul 04.
Artigo em Inglês | MEDLINE | ID: mdl-24925909

RESUMO

The peripheral autonomic nervous system reaches far throughout the body and includes neurons of diverse functions, such as sympathetic and parasympathetic. We show that the parasympathetic system in mice--including trunk ganglia and the cranial ciliary, pterygopalatine, lingual, submandibular, and otic ganglia--arise from glial cells in nerves, not neural crest cells. The parasympathetic fate is induced in nerve-associated Schwann cell precursors at distal peripheral sites. We used multicolor Cre-reporter lineage tracing to show that most of these neurons arise from bi-potent progenitors that generate both glia and neurons. This nerve origin places cellular elements for generating parasympathetic neurons in diverse tissues and organs, which may enable wiring of the developing parasympathetic nervous system.


Assuntos
Células-Tronco Neurais/citologia , Neurogênese , Neuroglia/citologia , Neurônios/citologia , Sistema Nervoso Parassimpático/embriologia , Animais , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Fatores de Transcrição Hélice-Alça-Hélice Básicos/metabolismo , Gânglios Parassimpáticos/citologia , Gânglios Parassimpáticos/embriologia , Camundongos , Camundongos Mutantes , Células-Tronco Neurais/metabolismo , Técnicas de Rastreamento Neuroanatômico/métodos , Neuroglia/metabolismo , Neurônios/metabolismo , Sistema Nervoso Parassimpático/citologia , Fatores de Transcrição SOXE/genética , Fatores de Transcrição SOXE/metabolismo , Células de Schwann/citologia , Células de Schwann/metabolismo
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