Clinical imaging in regenerative medicine

被引:191
作者
Naumova, Anna V. [1 ,2 ,3 ]
Modo, Michel [4 ,5 ,6 ,7 ]
Moore, Anna [8 ]
Murry, Charles E. [2 ,3 ,9 ,10 ,11 ]
Frank, Joseph A. [12 ,13 ]
机构
[1] Univ Washington, Dept Radiol, Seattle, WA 98195 USA
[2] Univ Washington, Ctr Cardiovasc Biol, Seattle, WA 98195 USA
[3] Univ Washington, Inst Stem Cell & Regenerat Med, Seattle, WA 98195 USA
[4] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA USA
[5] Univ Pittsburgh, Ctr Neural Basis Cognit, Pittsburgh, PA USA
[6] Univ Pittsburgh, Dept Radiol, Pittsburgh, PA 15260 USA
[7] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA USA
[8] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Dept Radiol, Charlestown, MA USA
[9] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[10] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
[11] Univ Washington, Dept Med Cardiol, Seattle, WA 98195 USA
[12] NIH, Bethesda, MD 20892 USA
[13] Natl Inst Biomed Imaging & Bioengn, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
NEURAL STEM-CELLS; POSITRON-EMISSION-TOMOGRAPHY; HEMATOPOIETIC PROGENITOR CELLS; IRON-OXIDE NANOPARTICLES; MARROW MONONUCLEAR-CELLS; NORMAL ORGAN WEIGHTS; IN-VIVO; MAGNETIC-RESONANCE; MYOCARDIAL-INFARCTION; ISLET TRANSPLANTATION;
D O I
10.1038/nbt.2993
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In regenerative medicine, clinical imaging is indispensable for characterizing damaged tissue and for measuring the safety and efficacy of therapy. However, the ability to track the fate and function of transplanted cells with current technologies is limited. Exogenous contrast labels such as nanoparticles give a strong signal in the short term but are unreliable long term. Genetically encoded labels are good both short-and long-term in animals, but in the human setting they raise regulatory issues related to the safety of genomic integration and potential immunogenicity of reporter proteins. Imaging studies in brain, heart and islets share a common set of challenges, including developing novel labeling approaches to improve detection thresholds and early delineation of toxicity and function. Key areas for future research include addressing safety concerns associated with genetic labels and developing methods to follow cell survival, differentiation and integration with host tissue. Imaging may bridge the gap between cell therapies and health outcomes by elucidating mechanisms of action through longitudinal monitoring.
引用
收藏
页码:804 / U121
页数:15
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