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1.
Odontology ; 110(2): 223-230, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-34807345

RESUMEN

Dissolution of hydroxyapatite from the tooth structure at low pH can lead to the irreversible destruction of enamel and dentin, which if left untreated can result in pain and tooth loss. Hydroxyapatite toothpastes contain hydroxyapatite particles in micro- or nanocrystalline form that have been shown to deposit and restore demineralized enamel surfaces. As such, they are currently being explored as a fluoride-free anti-caries agent. This narrative review article aims to summarize the recent findings of the research investigating the remineralization potential of HAP toothpaste in vitro, in situ and in vivo, as well as some other applications in dentistry.


Asunto(s)
Caries Dental , Pastas de Dientes , Cariostáticos/química , Cariostáticos/farmacología , Caries Dental/prevención & control , Durapatita/química , Fluoruros/farmacología , Humanos , Remineralización Dental , Pastas de Dientes/química
2.
Oncotarget ; 7(12): 13285-96, 2016 Mar 22.
Artículo en Inglés | MEDLINE | ID: mdl-26934440

RESUMEN

Hematopoietic stem and progenitor cell (HSPC) homeostasis declines with age, leading to impaired hematopoiesis. Mesenchymal stromal cells (MSC) are critical components of the bone marrow niche and key regulators of the balance between HSPC proliferation and quiescence. Accrual of DNA damage, a hallmark of cellular aging, occurs in aged MSC. Whether MSC aging alters the bone marrow niche triggering HSPC dysfunction is unknown. Using a human MSC-HSPC co-culture system, we demonstrated that DNA damaged MSC have impaired capacity to maintain CD34+CD38- HSPC quiescence. Furthermore, human MSC from adult donors display some hallmarks of cellular senescence and have a decreased capacity to maintain HSPC quiescence and the most primitive CD34+CD38- subset compared to MSC from pediatric donors. IL-6 neutralization restores the MSC-HPSC crosstalk in senescent and adult MSC-HSPC co-cultures highlighting the relevance of the local microenvironment in maintaining HSPC homeostasis. These results provide new evidence implicating components of the MSC secretome in HSPC aging.


Asunto(s)
Senescencia Celular/fisiología , Hematopoyesis/fisiología , Células Madre Hematopoyéticas/citología , Interleucina-6/metabolismo , Células Madre Mesenquimatosas/citología , Adolescente , Antígenos CD34/metabolismo , Apoptosis , Biomarcadores/metabolismo , Proliferación Celular , Células Cultivadas , Femenino , Células Madre Hematopoyéticas/metabolismo , Humanos , Masculino , Células Madre Mesenquimatosas/metabolismo , Persona de Mediana Edad
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