Poly(ADP-Ribose) Links the DNA Damage Response and Biomineralization
Author(s) -
Karin H. Müller,
Robert Hayward,
Rakesh Rajan,
Meredith Whitehead,
Andrew M. Cobb,
Sadia Ahmad,
Mengxi Sun,
Ieva Goldberga,
Rui Li,
Uliana Bashtanova,
Anna M. Puszkarska,
David G. Reid,
Roger A. Brooks,
Jeremy N. Skepper,
Jayanta Bordoloi,
Wing Ying Chow,
Hartmut Oschkinat,
Alexander S. Groombridge,
Oren A. Scherman,
James A. Harrison,
Anja Verhulst,
Patrick C. D’Haese,
Ellen Neven,
Lisa-Maria Needham,
Steven F. Lee,
Catherine M. Shanahan,
Melinda J. Duer
Publication year - 2019
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.05.038
Subject(s) - biomineralization , ribose , calcification , poly adp ribose polymerase , extracellular matrix , microbiology and biotechnology , extracellular , chemistry , biochemistry , in vitro , dna damage , mineralized tissues , biology , dna , polymerase , pathology , medicine , enzyme , paleontology , dentin
Summary Biomineralization of the extracellular matrix is an essential, regulated process. Inappropriate mineralization of bone and the vasculature has devastating effects on patient health, yet an integrated understanding of the chemical and cell biological processes that lead to mineral nucleation remains elusive. Here, we report that biomineralization of bone and the vasculature is associated with extracellular poly(ADP-ribose) synthesized by poly(ADP-ribose) polymerases in response to oxidative and/or DNA damage. We use ultrastructural methods to show poly(ADP-ribose) can form both calcified spherical particles, reminiscent of those found in vascular calcification, and biomimetically calcified collagen fibrils similar to bone. Importantly, inhibition of poly(ADP-ribose) biosynthesis in vitro and in vivo inhibits biomineralization, suggesting a therapeutic route for the treatment of vascular calcifications. We conclude that poly(ADP-ribose) plays a central chemical role in both pathological and physiological extracellular matrix calcification.
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