Your browser doesn't support javascript.
loading
Phylogeny and chemistry of biological mineral transport.
Schlesinger, Paul H; Braddock, Demetrios T; Larrouture, Quitterie C; Ray, Evan C; Riazanski, Vladimir; Nelson, Deborah J; Tourkova, Irina L; Blair, Harry C.
Afiliação
  • Schlesinger PH; Dept of Cell Biology, Washington University, Saint Louis, MO, United States of America.
  • Braddock DT; Dept. of Pathology, Yale New Haven Hospital, 310 Cedar Street, New Haven, CT, United States of America.
  • Larrouture QC; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, Windmill Road, Oxford OX3 7LD, UK.
  • Ray EC; Renal Electrolyte Division, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Riazanski V; Dept of Neurobiology, Pharmacology & Physiology, University of Chicago, Chicago, IL, United States of America.
  • Nelson DJ; Dept of Neurobiology, Pharmacology & Physiology, University of Chicago, Chicago, IL, United States of America.
  • Tourkova IL; Veteran's Affairs Medical Center, Pittsburgh PA and Department of Pathology, University of Pittsburgh, Pittsburgh, PA, United States of America.
  • Blair HC; Veteran's Affairs Medical Center, Pittsburgh PA and Department of Pathology, University of Pittsburgh, Pittsburgh, PA, United States of America. Electronic address: hcblair@imap.pitt.edu.
Bone ; 141: 115621, 2020 12.
Article em En | MEDLINE | ID: mdl-32858255
Three physiologically mineralizing tissues - teeth, cartilage and bone - have critical common elements and important evolutionary relationships. Phylogenetically the most ancient densely mineralized tissue is teeth. In jawless fishes without skeletons, tooth formation included epithelial transport of phosphates, a process echoed later in bone physiology. Cartilage and mineralized cartilage are skeletal elements separate from bone, but with metabolic features common to bone. Cartilage mineralization is coordinated with high expression of tissue nonspecific alkaline phosphatase and PHOSPHO1 to harvest available phosphate esters and support mineralization of collagen secreted locally. Mineralization in true bone results from stochastic nucleation of hydroxyapatite crystals within the cross-linked collagen fibrils. Mineral accumulation in dense collagen is, at least in major part, mediated by amorphous aggregates - often called Posner clusters - of calcium and phosphate that are small enough to diffuse into collagen fibrils. Mineral accumulation in membrane vesicles is widely suggested, but does not correlate with a definitive stage of mineralization. Conversely mineral deposition at non-physiologic sites where calcium and phosphate are adequate has been shown to be regulated in large part by pyrophosphate. All of these elements are present in vertebrate bone metabolism. A key biological element of bone formation is an epithelial-like cellular organization which allows control of phosphate, calcium and pH during mineralization.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osso e Ossos / Calcificação Fisiológica Idioma: En Revista: Bone Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osso e Ossos / Calcificação Fisiológica Idioma: En Revista: Bone Ano de publicação: 2020 Tipo de documento: Article