Published November 22, 2023 | Version v1
Journal article Open

Epithelial-like transport of mineral distinguishes bone formation from other connective tissues

  • 1. Veteran's Affairs Medical Center
  • 2. University of Pittsburgh
  • 3. University of Chicago
  • 4. Washington University in Saint Louis

Description

We review unique properties of bone formation including current understanding of mechanisms of bone mineral transport. We focus on formation only; mechanism of bone degradation is a separate topic not considered. Bone matrix is compared to other connective tissues composed mainly of the same proteins, but without the specialized mechanism for continuous transport and deposition of mineral. Indeed other connective tissues add mechanisms to prevent mineral formation. We start with the epithelial-like surfaces that mediate transport of phosphate to be incorporated into hydroxyapatite in bone, or in its ancestral tissue, the tooth. These include several phosphate producing or phosphate transport-related proteins with special expression in large quantities in bone, particularly in the bone-surface osteoblasts. In all connective tissues including bone, the proteins that constitute the protein matrix are mainly type I collagen and γ−carboxylate-containing small proteins in similar molar quantities to collagen. Specialized proteins that regulate connective tissue structure and formation are surprisingly similar in mineralized and non-mineralized tissues. While serum calcium and phosphate are adequate to precipitate mineral, specialized mechanisms normally prevent mineral formation except in bone, where continuous transport and deposition of mineral occurs.

Data availability

Data sharing is not applicable to this article as no new data were created or analyzed in this study.

Files

Epithelial-like-transport-of-mineral-distinguishes-bone-formation-from-other-connective-tissues.pdf

Additional details

Identifiers

DOI
10.1002/jcb.30494
Other
oai:uchicago.tind.io:9809

Funding

National Institutes of Health
1 R01 AR076146-01
Department of Veteran's Affairs
BX002490-06A1

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Neurobiology, Pharmacological and Physiological Sciences