4.5 Review

Matrix vesicles from chondrocytes and osteoblasts: Their biogenesis, properties, functions and biomimetic models

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
Volume 1862, Issue 3, Pages 532-546

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbagen.2017.11.005

Keywords

Mineralization; Matrix vesicles; Lipid raft; Proteoliposomes; Atomic force microscopy; Electron microscopy

Funding

  1. National Institute of General Medical Sciences [R01CA179087, R01GM115972]
  2. FAPESP [2016/21236-0, 2014/11941-3, 2014/00371-1]
  3. CAPES
  4. CNPq
  5. FAPESP
  6. Polonium grant [33540RG]

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Background: Matrix vesicles (MVs) are released from hypertrophic chondrocytes and from mature osteoblasts, the cells responsible for endochondral and membranous ossification. Under pathological conditions, they can also be released from cells of non-skeletal tissues such as vascular smooth muscle cells. MVs are extracellular vesicles of approximately 100-300 nm diameter harboring the biochemical machinery needed to induce mineralization. Scope of the review: The review comprehensively delineates our current knowledge of MV biology and highlights open questions aiming to stimulate further research. The review is constructed as a series of questions addressing issues of MVs ranging from their biogenesis and functions, to biomimetic models. It critically evaluates experimental data including their isolation and characterization methods, like lipidomics, proteomics, transmission electron microscopy, atomic force microscopy and proteoliposome models mimicking MVs. Major conclusions: MVs have a relatively well-defined function as initiators of mineralization. They bind to collagen and their composition reflects the composition of lipid rafts. We call attention to the as yet unclear mechanisms leading to the biogenesis of MVs, and how minerals form and when they are formed. We discuss the prospects of employing upcoming experimental models to deepen our understanding of MV-mediated mineralization and mineralization disorders such as the use of reconstituted lipid vesicles, proteoliposomes and, native sample preparations and high-resolution technologies.

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