Noninvasive Monitoring of Allogeneic Stem Cell Delivery with Dual-Modality Imaging-Visible Microcapsules in a Rabbit Model of Peripheral Arterial Disease

Joint Authors

Gabrielson, Kathleen L.
Wacker, Frank
Fu, Yingli
Weiss, Clifford R.
Kedziorek, Dorota A.
Xie, Yibin
Tully, Ellen
Shea, Steven M.
Solaiyappan, Meiyappan
Ehtiati, Tina
Bulte, Jeff W. M.
Kraitchman, Dara L.

Source

Stem Cells International

Issue

Vol. 2019, Issue 2019 (31 Dec. 2019), pp.1-10, 10 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2019-03-14

Country of Publication

Egypt

No. of Pages

10

Abstract EN

Stem cell therapies, although promising for treating peripheral arterial disease (PAD), often suffer from low engraftment rates and the inability to confirm the delivery success and track cell distribution and engraftment.

Stem cell microencapsulation combined with imaging contrast agents may provide a means to simultaneously enhance cell survival and enable cell tracking with noninvasive imaging.

Here, we have evaluated a novel MRI- and X-ray-visible microcapsule formulation for allogeneic mesenchymal stem cell (MSC) delivery and tracking in a large animal model.

Bone marrow-derived MSCs from male New Zealand White rabbits were encapsulated using a modified cell encapsulation method to incorporate a dual-modality imaging contrast agent, perfluorooctyl bromide (PFOB).

PFOB microcapsules (PFOBCaps) were then transplanted into the medial thigh of normal or PAD female rabbits.

In vitro MSC viability remained high (79±5% at 4 weeks of postencapsulation), and as few as two and ten PFOBCaps could be detected in phantoms using clinical C-arm CT and 19F MRI, respectively.

Successful injections of PFOBCaps in the medial thigh of normal (n=15) and PAD (n=16) rabbits were demonstrated on C-arm CT at 1-14 days of postinjection.

Using 19F MRI, transplanted PFOBCaps were clearly identified as “hot spots” and showed one-to-one correspondence to the radiopacities on C-arm CT.

Concordance of 19F MRI and C-arm CT locations of PFOBCaps with postmortem locations was high (95%).

Immunohistological analysis revealed high MSC survival in PFOBCaps (>56%) two weeks after transplantation while naked MSCs were no longer viable beyond three days after delivery.

These findings demonstrate that PFOBCaps could maintain cell viability even in the ischemic tissue and provide a means to monitor cell delivery and track engraftment using clinical noninvasive imaging systems.

American Psychological Association (APA)

Fu, Yingli& Weiss, Clifford R.& Kedziorek, Dorota A.& Xie, Yibin& Tully, Ellen& Shea, Steven M.…[et al.]. 2019. Noninvasive Monitoring of Allogeneic Stem Cell Delivery with Dual-Modality Imaging-Visible Microcapsules in a Rabbit Model of Peripheral Arterial Disease. Stem Cells International،Vol. 2019, no. 2019, pp.1-10.
https://search.emarefa.net/detail/BIM-1210083

Modern Language Association (MLA)

Fu, Yingli…[et al.]. Noninvasive Monitoring of Allogeneic Stem Cell Delivery with Dual-Modality Imaging-Visible Microcapsules in a Rabbit Model of Peripheral Arterial Disease. Stem Cells International No. 2019 (2019), pp.1-10.
https://search.emarefa.net/detail/BIM-1210083

American Medical Association (AMA)

Fu, Yingli& Weiss, Clifford R.& Kedziorek, Dorota A.& Xie, Yibin& Tully, Ellen& Shea, Steven M.…[et al.]. Noninvasive Monitoring of Allogeneic Stem Cell Delivery with Dual-Modality Imaging-Visible Microcapsules in a Rabbit Model of Peripheral Arterial Disease. Stem Cells International. 2019. Vol. 2019, no. 2019, pp.1-10.
https://search.emarefa.net/detail/BIM-1210083

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1210083