TY - JOUR
T1 - A permanent window for the murine lung enables high-resolution imaging of cancer metastasis
AU - Entenberg, David
AU - Voiculescu, Sonia
AU - Guo, Peng
AU - Borriello, Lucia
AU - Wang, Yarong
AU - Karagiannis, George S.
AU - Jones, Joan
AU - Baccay, Francis
AU - Oktay, Maja
AU - Condeelis, John
N1 - Funding Information:
This technology was developed in the Gruss-Lipper Biophotonics Center and the Integrated Imaging Program at Albert Einstein College of Medicine. We acknowledge the support of these Centers in this work: Einstein’s Integrated Imaging Program, Montefiore’s Ruth L. Kirschstein T32 Training Grant of Surgeons for the Study of the Tumor Microenvironment (CA200561), NIH grants CA100324, CA216248, P30CA013330, and SIG #1S10OD019961-01. We thank M. Rottenkolber, R. Ibagon and A. Leggiadro of the Einstein Machine Shop for their skilled craftsmanship and design insight; and we thank C. Rodriguez-Tirado, B. Canella and U. Steidl’s lab for help with evaluating blood counts.
PY - 2018/1/3
Y1 - 2018/1/3
N2 - Stable, high-resolution intravital imaging of the lung has become possible through the utilization of vacuum-stabilized imaging windows. However, this technique is extremely invasive and limited to only hours in duration. Here we describe a minimally invasive, permanently implantable window for high-resolution intravital imaging of the murine lung that allows the mouse to survive surgery, recover from anesthesia, and breathe independently. Compared to vacuum-stabilized windows, this window produces the same high-quality images without vacuum-induced artifacts; it is also less invasive, which allows imaging of the same lung tissue over a period of weeks. We further adapt the technique of microcartography for reliable relocalization of the same cells longitudinally. Using commonly employed experimental, as well as more clinically relevant, spontaneous metastasis models, we visualize all stages of metastatic seeding, including: tumor cell arrival; extravasation; growth and progression to micrometastases; as well as tumor microenvironment of metastasis function, the hallmark of hematogenous dissemination of tumor cells.
AB - Stable, high-resolution intravital imaging of the lung has become possible through the utilization of vacuum-stabilized imaging windows. However, this technique is extremely invasive and limited to only hours in duration. Here we describe a minimally invasive, permanently implantable window for high-resolution intravital imaging of the murine lung that allows the mouse to survive surgery, recover from anesthesia, and breathe independently. Compared to vacuum-stabilized windows, this window produces the same high-quality images without vacuum-induced artifacts; it is also less invasive, which allows imaging of the same lung tissue over a period of weeks. We further adapt the technique of microcartography for reliable relocalization of the same cells longitudinally. Using commonly employed experimental, as well as more clinically relevant, spontaneous metastasis models, we visualize all stages of metastatic seeding, including: tumor cell arrival; extravasation; growth and progression to micrometastases; as well as tumor microenvironment of metastasis function, the hallmark of hematogenous dissemination of tumor cells.
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U2 - 10.1038/nmeth.4511
DO - 10.1038/nmeth.4511
M3 - Article
C2 - 29176592
AN - SCOPUS:85040165795
SN - 1548-7091
VL - 15
SP - 73
EP - 80
JO - Nature Methods
JF - Nature Methods
IS - 1
ER -