Intercellular pathways from the vasculature to the forming bone in the zebrafish larval caudal fin: Possible role in bone formation.


Journal

Journal of structural biology
ISSN: 1095-8657
Titre abrégé: J Struct Biol
Pays: United States
ID NLM: 9011206

Informations de publication

Date de publication:
01 05 2019
Historique:
received: 09 11 2018
revised: 23 02 2019
accepted: 25 02 2019
pubmed: 13 3 2019
medline: 20 6 2020
entrez: 13 3 2019
Statut: ppublish

Résumé

The pathway of ion supply from the source to the site of bone deposition in vertebrates is thought to involve transport through the vasculature, followed by ion concentration in osteoblasts. The cells deposit a precursor mineral phase in vesicles, which are then exocytosed into the extracellular matrix. We observed that the entire skeleton of zebrafish larvae, is labelled within minutes after injection of calcein or FITC-dextran into the blood. This raised the possibility that there is an additional pathway of solute transport that can account for the rapid labelling. We used cryo-FIB-SEM serial block face imaging to reconstruct at high resolution the 3D ultrastructure of the caudal tail of the zebrafish larva. This reconstruction clearly shows that there is a continuous intercellular pathway from the artery to the forming bone, and from the forming bone to the vein. Fluorescence light microscopy shows that calcein and FITC-dextran form a reticulate network pattern in this tissue, which we attribute to the dye being present in the intercellular space. We conclude that this intercellular continuous space may be a supply route for ions, mineral and other solute or particulate material to the fast forming bone.

Identifiants

pubmed: 30858049
pii: S1047-8477(19)30045-0
doi: 10.1016/j.jsb.2019.02.011
pii:
doi:

Substances chimiques

Coloring Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

139-148

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Anat Akiva (A)

Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel; Laboratory of Materials and Interface Chemistry and Center for Multiscale Electron Microscopy, Department of Chemical Engineering and Chemistry and Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, the Netherlands.

Or Nelkenbaum (O)

Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.

Andreas Schertel (A)

Carl Zeiss Microscopy GmbH, Global Applications Support, Oberkochen, Germany.

Karina Yaniv (K)

Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.

Steve Weiner (S)

Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.

Lia Addadi (L)

Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel. Electronic address: Lia.addadi@weizmann.ac.il.

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