Imaging Macrophage and Hematopoietic Progenitor Proliferation in Atherosclerosis

Research output: Contribution to journalJournal articleResearchpeer-review

  • Yu-Xiang Ye
  • Claudia Calcagno
  • Gabriel Courties
  • Edmund J Keliher
  • Gregory R Wojtkiewicz
  • Yoshiko Iwamoto
  • Jun Tang
  • Carlos Pérez-Medina
  • Venkatesh Mani
  • Seigo Ishino
  • Camilla Bardram Johnbeck
  • Ulrich Knigge
  • Zahi A Fayad
  • Peter Libby
  • Ralph Weissleder
  • Ahmed Tawakol
  • Shipra Dubey
  • Anthony P Belanger
  • Marcelo F Di Carli
  • Filip K Swirski
  • Willem J M Mulder
  • Matthias Nahrendorf

RATIONALE: Local plaque macrophage proliferation and monocyte production in hematopoietic organs promote progression of atherosclerosis. Therefore, noninvasive imaging of proliferation could serve as a biomarker and monitor therapeutic intervention.

OBJECTIVE: To explore (18)F-FLT positron emission tomography-computed tomography imaging of cell proliferation in atherosclerosis.

METHODS AND RESULTS: (18)F-FLT positron emission tomography-computed tomography was performed in mice, rabbits, and humans with atherosclerosis. In apolipoprotein E knock out mice, increased (18)F-FLT signal was observed in atherosclerotic lesions, spleen, and bone marrow (standardized uptake values wild-type versus apolipoprotein E knock out mice, 0.05 ± 0.01 versus 0.17 ± 0.01, P<0.05 in aorta; 0.13 ± 0.01 versus 0.28 ± 0.02, P<0.05 in bone marrow; 0.06 ± 0.01 versus 0.22 ± 0.01, P<0.05 in spleen), corroborated by ex vivo scintillation counting and autoradiography. Flow cytometry confirmed significantly higher proliferation of macrophages in aortic lesions and hematopoietic stem and progenitor cells in the spleen and bone marrow in these mice. In addition, (18)F-FLT plaque signal correlated with the duration of high cholesterol diet (r(2)=0.33, P<0.05). Aortic (18)F-FLT uptake was reduced when cell proliferation was suppressed with fluorouracil in apolipoprotein E knock out mice (P<0.05). In rabbits, inflamed atherosclerotic vasculature with the highest (18)F-fluorodeoxyglucose uptake enriched (18)F-FLT. In patients with atherosclerosis, (18)F-FLT signal significantly increased in the inflamed carotid artery and in the aorta.

CONCLUSIONS: (18)F-FLT positron emission tomography imaging may serve as an imaging biomarker for cell proliferation in plaque and hematopoietic activity in individuals with atherosclerosis.

Original languageEnglish
JournalCirculation Research
Volume117
Issue number10
Pages (from-to)835-45
Number of pages11
ISSN0009-7330
DOIs
Publication statusPublished - 2015

    Research areas

  • Animals, Aorta, Thoracic, Aortic Diseases, Apolipoproteins E, Atherosclerosis, Bone Marrow, Carotid Artery Diseases, Cell Proliferation, Cholesterol, Dietary, Dideoxynucleosides, Diet, High-Fat, Disease Models, Animal, Female, Fluorodeoxyglucose F18, Hematopoietic Stem Cells, Humans, Macrophages, Male, Mice, Inbred C57BL, Mice, Knockout, Multimodal Imaging, Plaque, Atherosclerotic, Positron-Emission Tomography, Predictive Value of Tests, Rabbits, Radiopharmaceuticals, Retrospective Studies, Spleen, Time Factors, Tomography, X-Ray Computed

ID: 162683446