Development and characterization of supramolecular calcitonin assembly and assessment of its interactions with the bone remodelling process

Bone. 2019 May:122:123-135. doi: 10.1016/j.bone.2019.02.019. Epub 2019 Feb 21.

Abstract

Osteoporosis is the most common metabolic bone disease, which poses an immense socio-economic burden on the society. Human calcitonin, though safe, is not considered as a therapeutic option because of its high tendency to self-associate to form amyloid fibrils thereby affecting its potency. To circumvent this issue we harnessed the inherent capacity of aggregation and developed an assemblage of human calcitonin monomers, [Supramolecular Calcitonin Assembly (SCAI)], which releases biologically active calcitonin monomers in a sustained manner for a period of at least three weeks. AFM and FT-IR analysis showed that SCA-I is amorphous aggregates of calcitonin monomers. Both SCA-I and monomer released from it demonstrated superior anti-osteoclast activity and proteolytic stability in-vitro. SCA-I upon single injection significantly improved bone formation markers and reduced bone resorption markers in ovariectomized (OVX) rat model of postmenopausal osteoporosis. Micro-CT analysis revealed that calcitonin released from SCA-I exhibits its beneficial effect on cortical bone more profoundly compared to trabecular bone. This study demonstrates that SCA-I is more effective compared to the human calcitonin monomers on osteoclasts and has site-specific effect on bone in a model of post-menopausal osteoporosis. This approach opens up an innovative way to use and study the function of human calcitonin.

Keywords: Human calcitonin; Osteoporosis; Ovariectomy; Protein aggregation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biophysical Phenomena
  • Bone Remodeling*
  • Bone Resorption / blood
  • Bone Resorption / pathology
  • Calcitonin / metabolism*
  • Disease Models, Animal
  • Female
  • Femur / diagnostic imaging
  • Humans
  • Mice
  • Osteocalcin / genetics
  • Osteocalcin / metabolism
  • Osteoclasts / metabolism
  • Postmenopause / blood
  • RAW 264.7 Cells
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats, Sprague-Dawley
  • X-Ray Microtomography

Substances

  • RNA, Messenger
  • Osteocalcin
  • Calcitonin