DEL-1 restrains osteoclastogenesis and inhibits inflammatory bone loss in nonhuman primates

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Jieun Shin - , University of Michigan, Ann Arbor (Autor:in)
  • Tomoki Maekawa - , University of Michigan, Ann Arbor (Autor:in)
  • Toshiharu Abe - , University of Michigan, Ann Arbor (Autor:in)
  • Evlambia Hajishengallis - , University of Pennsylvania (Autor:in)
  • Kavita Hosur - , University of Michigan, Ann Arbor (Autor:in)
  • Kalyani Pyaram - , University of Michigan, Ann Arbor (Autor:in)
  • Ioannis Mitroulis - , Institut für Klinische Chemie und Laboratoriumsmedizin (Autor:in)
  • Triantafyllos Chavakis - , Institut für Klinische Chemie und Laboratoriumsmedizin (Autor:in)
  • George Hajishengallis - , University of Michigan, Ann Arbor (Autor:in)

Abstract

DEL-1 (developmental endothelial locus-1) is an endothelial cell-secreted protein that regulates LFA-1 (lymphocyte function-associated antigen-1) integrin-dependent leukocyte recruitment and inflammation in various tissues. We identified a novel regulatory mechanism of DEL-1 in osteoclast biology. Specifically, we showed that DEL-1 is expressed by human and mouse osteoclasts and regulates their differentiation and resorptive function. Mechanistically, DEL-1 inhibited the expression of NFATc1, a master regulator of osteoclastogenesis, in a Mac-1 integrin- dependentmanner. In vivo mechanistic analysis has dissociated the anti-inflammatory from the anti-bone-resorptive action of DEL-1 and identified structural components thereof mediating these distinct functions. Locally administered human DEL-1 blocked inflammatory periodontal bone loss in nonhuman primates-a relevantmodel of human periodontitis. The ability of DEL-1 to regulate both upstream (inflammatory cell recruitment) and downstream (osteoclastogenesis) events that lead to inflammatory bone loss paves the way to a new class of endogenous therapeutics for treating periodontitis and perhaps other inflammatory disorders.

Details

OriginalspracheEnglisch
Aufsatznummer307ra155
FachzeitschriftScience Translational Medicine
Jahrgang7
Ausgabenummer307
PublikationsstatusVeröffentlicht - 30 Sept. 2015
Peer-Review-StatusJa

Externe IDs

researchoutputwizard legacy.publication#66928
Scopus 84942881294
PubMed 26424570

Schlagworte

ASJC Scopus Sachgebiete