Discovery of a bone-like blood particle in the peripheral circulation of humans and rodents

Microcirculation. 2019 Nov;26(8):e12579. doi: 10.1111/micc.12579. Epub 2019 Jul 21.

Abstract

Objective: To characterize ossified bone marrow blood vessels and confirm the presence of ossified particles (OSP) in humans and rodents.

Methods: Human bone marrow blood vessels were processed for scanning and transmission electron microscopy. Whole blood samples were collected from younger (26-39 years; n = 6) and older (55-63 years; n = 6) volunteers and male Fischer-344 rats (1 month, n = 7; 6 months, n = 7; 12 months, n = 7; 18-months, n = 6; 24 months, n = 8). OSP in the whole blood samples were sorted and imaged with microscopy to determine diameter, circularity, and solidity. Additionally, the chemical composition of OSP was determined via elemental analysis.

Results: SEM revealed two types of ossified bone marrow blood vessels: that is, "transitioning" and "ossified." OSP were adhered to the surface of transitioning vessels and theoretically gain access to and circulate within the blood. The majority of OSP were ≤15 μm in diameter, but many were of sufficient size to serve as emboli (ie, >15 μm).OSP were predominately oblong in shape and several had jagged tips and edges.

Conclusions: We introduce a novel, bone-like blood particle that may be diagnostic of bone marrow blood vessel ossification. Further, OSP may associate with several disease states (eg, atherosclerosis).

Keywords: bone marrow blood vessel ossification; emboli; human; ossified particles; rat.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Bone Marrow Diseases* / blood
  • Bone Marrow Diseases* / pathology
  • Bone Marrow* / blood supply
  • Bone Marrow* / ultrastructure
  • Extracellular Vesicles* / metabolism
  • Extracellular Vesicles* / ultrastructure
  • Female
  • Humans
  • Male
  • Middle Aged
  • Ossification, Heterotopic* / blood
  • Ossification, Heterotopic* / pathology
  • Rats
  • Rats, Inbred F344
  • Vascular Calcification* / blood
  • Vascular Calcification* / pathology