Gimi Barjor, Artemov Dmitri, Leong Timothy, Gracias David H, Gilson Wesley, Stuber Matthias, Bhujwalla Zaver M
Department of Radiology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75062, USA.
Cell Transplant. 2007;16(4):403-8. doi: 10.3727/000000007783464803.
Several molecular therapies require the implantation of cells that secrete biotherapeutic molecules and imaging the location and microenvironment of the cellular implant to ascertain its function. We demonstrate noninvasive in vivo magnetic resonance imaging (MRI) of self-assembled microcontainers that are capable of cell encapsulation. Negative contrast was obtained to discern the microcontainer with MRI; positive contrast was obtained in the complete absence of background signal. MRI on a clinical scanner highlights the translational nature of this research. The microcontainers were loaded with cells that were dispersed in an extracellular matrix, and implanted both subcutaneously and in human tumor xenografts in SCID mice. MRI was performed on the implants, and microcontainers retrieved postimplantation showed cell viability both within and proximal to the implant. The microcontainers are characterized by their small size, three dimensionality, controlled porosity, ease of parallel fabrication, chemical and mechanical stability, and noninvasive traceability in vivo.
几种分子疗法需要植入能分泌生物治疗分子的细胞,并对细胞植入物的位置和微环境进行成像,以确定其功能。我们展示了能够封装细胞的自组装微容器的无创体内磁共振成像(MRI)。通过MRI获得负性对比以辨别微容器;在完全没有背景信号的情况下获得正性对比。临床扫描仪上的MRI突出了这项研究的转化性质。微容器装载有分散在细胞外基质中的细胞,并皮下植入以及植入SCID小鼠的人肿瘤异种移植物中。对植入物进行MRI检查,植入后取出的微容器显示植入物内部及其近端的细胞活力。微容器的特点是尺寸小、三维结构、孔隙率可控、易于平行制造、化学和机械稳定性以及体内无创可追溯性。