journal article·2020-06

Fluorescent conjugated polymer nanovector for in vivo tracking and regulating the fate of stem cells for restoring infarcted myocardium

Guorui Jin, Wenfang Li, Fan Song, Jing Zhao, Mengqi Wang, Qian Liu, Ang Li, Guoyou Huang, Feng Xu

Acta Biomaterialia· Volume 109
Publisher page

Abstract

Stem cell therapy holds great promise for cardiac regeneration. However, the lack of ability to control stem cell fate after in vivo transplantation greatly restricts its therapeutic outcomes. MicroRNA delivery has emerged as a powerful tool to control stem cell fate for enhanced cardiac regeneration. However, the clinical translation of therapy based on gene-transfected stem cells remains challenging, due to the unknown in vivo behaviors of stem cells. Here, we developed a nano-platform (i.e., PFBT@miR-1-Tat NPs) that can achieve triggered release of microRNA-1 to promote cardiac differentiation of mesenchymal stem cells (MSCs), and long-term tracking of transplanted MSCs through bright and ultra-stable fluorescence of conjugated polymer poly(9,9-dioctylfluorene-alt-benzothiadiazole) (PFBT). We found that PFBT@miR-1-Tat NP-treated MSCs significantly restored the infarcted myocardium by promoting stem cell cardiac differentiation and integration with the in situ cardiac tissues. Meanwhile, MSCs without gene delivery improved the infarcted heart functions mainly through a paracrine effect and blood vessel formation. The developed conjugated polymer nanovector should be a powerful tool for manipulating as well as revealing the fate of therapeutic cells in vivo, which is critical for optimizing the therapeutic route of gene and cell combined therapy and therefore for accelerating clinical translation. STATEMENT OF SIGNIFICANCE: The lack of controllability in stem cell fate and the unclear in vivo cellular behaviors restrict the therapeutic outcomes of stem cell therapy. Herein, we engineered fluorescent conjugated polymer nanoparticles as gene delivery nanovectors with controlled release and high intracellular delivery capability to harness the fate of mesenchymal stem cells (MSCs) in vivo, meanwhile to reveal the cellular mechanism of gene-treated stem cell therapy. As compared with only MSC treatment that improves infarcted myocardium functions through paracrine effect, treatment with conjugated polymer nanovector-treated MSCs significantly restored infarcted myocardium through enhancing MSC cardiac differentiation and integration with the in-situ cardiac tissues. These findings demonstrate that the conjugated polymer nanovector would be a powerful tool in optimizing gene and cell combined therapy.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Tissue Engineering and Regenerative Medicine · Electrospun Nanofibers in Biomedical Applications · RNA Interference and Gene Delivery

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (64)

Show source-provided references
1. Executive summary: heart disease and stroke statistics—2016 update10.1161/CIR.0000000000000366 ↗
2. Heart regeneration: opportunities and challenges for drug discovery with novel chemical and therapeutic methods or agents10.1002/anie.201307034 ↗
3. Cell therapy for heart failure10.1161/CIRCRESAHA.113.300219 ↗
4. Reprogramming toward heart regeneration: stem cells and beyond10.1016/j.stem.2013.02.008 ↗
5. MicroRNA-1 transfected embryonic stem cells enhance cardiac myocyte differentiation and inhibit apoptosis by modulating the PTEN/Akt pathway in the infarcted heart10.1152/ajpheart.00271.2011 ↗
6. Intravenous injection of allogeneic umbilical cord-derived multipotent mesenchymal stromal cells reduces the infarct area and ameliorates cardiac function in a porcine model of acute myocardial infarction10.1186/s13287-018-0888-z ↗
7. Autologous preconditioned mesenchymal stem cell sheets improve left ventricular function in a rabbit old myocardial infarction model
8. Interaction between myofibroblasts and stem cells in the fibrotic heart: balancing between deterioration and regeneration10.1093/cvr/cvu047 ↗
9. Clarifying stem-cell therapy's benefits and risks10.1056/NEJMp1613723 ↗
10. Human msc suppression correlates with cytokine induction of Indoleamine 2,3-Dioxygenase and bystander M2 macrophage differentiation10.1038/mt.2011.189 ↗
11. Stem-cell therapy for cardiac disease10.1038/nature06800 ↗
12. Myocardial regeneration: roles of stem cells and hydrogels10.1016/j.addr.2011.02.007 ↗
13. Characterization and enrichment of cardiomyocytes derived from human embryonic stem cells10.1161/01.RES.0000035254.80718.91 ↗
14. Use of adult marrow mesenchymal stem cells for regeneration of cardiomyocytes10.1038/sj.bmt.1703940 ↗
15. TGF beta 1 contributes to cardiomyogenic-like differentiation of human bone marrow mesenchymal stem cells10.1016/j.ijcard.2011.08.003 ↗
16. Transient inhibition of bmp signaling by noggin induces cardiomyocyte differentiation of mouse embryonic stem cells10.1038/nbt0705-897b ↗
17. Clinical outcome 2 years after intracoronary administration of bone marrow-derived progenitor cells in acute myocardial infarction10.1161/CIRCHEARTFAILURE.108.843243 ↗
18. Electrical stimulation of human embryonic stem cells: cardiac differentiation and the generation of reactive oxygen species10.1016/j.yexcr.2009.08.015 ↗
19. Differentiation of human embryonic stem cells to cardiomyocytes10.1161/01.CIR.0000068356.38592.68 ↗
20. Human cardiovascular progenitor cells develop from a KDR+ embryonic-stem-cell-derived population10.1038/nature06894 ↗
21. Stage-Specific optimization of activin/nodal and bmp signaling promotes cardiac differentiation of mouse and human pluripotent stem cell lines10.1016/j.stem.2010.12.008 ↗
22. Human pluripotent stem cells: prospects and challenges as a source of cardiomyocytes for in vitro modeling and cell-based cardiac repair10.1016/j.addr.2015.05.004 ↗
23. Extracellular matrix promotes highly efficient cardiac differentiation of human pluripotent stem cells the matrix sandwich method10.1161/CIRCRESAHA.112.273144 ↗
24. Small changes can make a big difference — Microrna regulation of cardiac hypertrophy10.1016/j.yjmcc.2011.09.015 ↗
25. A microRNA-Hippo pathway that promotes cardiomyocyte proliferation and cardiac regeneration in mice10.1126/scitranslmed.3010841 ↗
26. MicroRNAs in stem cell function and regenerative therapy of the heart, arterioscler10.1161/ATVBAHA.113.300138 ↗
27. ES cells overexpressing microRNA-1 attenuate apoptosis in the injured myocardium10.1007/s11010-011-0883-5 ↗
28. Ultrafast fluorescence imaging in vivo with conjugated polymer fluorophores in the second near-infrared window10.1038/ncomms5206 ↗
29. Increasing the efficacy of stem cell therapy via triple-function inorganic nanoparticles10.1021/acsnano.9b00653 ↗
30. In vivo tracking techniques for cellular regeneration, replacement, and redirection10.2967/jnumed.112.106146 ↗
31. Development of a trimodal contrast agent for acoustic and magnetic particle imaging of stem cells10.1021/acsanm.8b00063 ↗
32. Photostable fluorescent organic dots with aggregation-induced emission (AIE dots) for noninvasive long-term cell tracing10.1038/srep01150 ↗
33. Tracking the engraftment and regenerative capabilities of transplanted lung stem cells using fluorescent nanodiamonds10.1038/nnano.2013.147 ↗
34. Noninvasive cell-tracking methods10.1038/nrclinonc.2011.141 ↗
35. Clinical imaging in regenerative medicine10.1038/nbt.2993 ↗
36. Semiconducting polymer nanoprobe for in vivo imaging of reactive oxygen and nitrogen species10.1002/anie.201303420 ↗
37. The cytotoxicity of CdTe quantum dots and the relative contributions from released cadmium ions and nanoparticle properties10.1016/j.biomaterials.2010.02.074 ↗
38. Polymer-encapsulated organic nanoparticles for fluorescence and photoacoustic imaging10.1039/C4CS00014E ↗
39. Conjugated polymer based nanoparticles as dual-modal probes for targeted in vivo fluorescence and magnetic resonance imaging10.1002/adfm.201102234 ↗
40. Amplified energy transfer in conjugated polymer nanoparticle tags and sensors10.1039/c0nr00322k ↗
41. Targeted co-delivery of docetaxel and siPlk1 by herceptin-conjugated vitamin E TPGS based immunomicelles10.1016/j.biomaterials.2013.01.009 ↗
42. Recent progress in microRNA delivery for cancer therapy by non-viral synthetic vectors10.1016/j.addr.2014.10.031 ↗
43. Multifunctional organic nanoparticles with aggregation-induced emission (AIE) characteristics for targeted photodynamic therapy and RNA interference therapy10.1039/C5CC07818K ↗
44. The protective effects of acupoint gel embedding on rats with myocardial ischemia-reperfusion injury10.1016/j.lfs.2018.09.010 ↗
45. Fluorescent polymer nanoparticles based on dyes: seeking brighter tools for bioimaging10.1002/smll.201503396 ↗
46. Photoluminescent and biodegradable polycitrate-polyethylene glycol-polyethyleneimine polymers as highly biocompatible and efficient vectors for bioimaging-guided siRNA and miRNA delivery10.1016/j.actbio.2017.02.034 ↗
47. NIR-I-to-NIR-II fluorescent nanomaterials for biomedical imaging and cancer therapy10.1039/C7TB02573D ↗
48. Advances in lipid-lowering therapy through gene-silencing technologies10.1038/nrcardio.2018.3 ↗
49. Amine-functionalized SiO2 nanodot-coated layered double hydroxide nanocomposites for enhanced gene delivery10.1007/s12274-014-0552-6 ↗
50. Concise review: mesenchymal stem cells: their phenotype, differentiation capacity, immunological features, and potential for homing10.1634/stemcells.2007-0197 ↗
51. Nanotoxicity assessment of quantum dots: from cellular to primate studies10.1039/C2CS35392J ↗
52. Gene therapy for heart failure: new perspectives10.1007/s11897-018-0410-z ↗
53. Evaluation of oxidative stress in autism: defective antioxidant enzymes and increased lipid peroxidation10.1007/s12011-010-8840-9 ↗
54. Conjugated polymer nanodots as ultrastable long-term trackers to understand mesenchymal stem cell therapy in skin regeneration10.1002/adfm.201501081 ↗
55. miR-1 association with cell proliferation inhibition and apoptosis in vestibular Schwannoma by targeting VEGFA10.4238/gmr15048923 ↗
56. Overexpression of microRNA-1 promotes cardiomyocyte commitment from human cardiovascular progenitors via suppressing WNT and FGF signaling pathways10.1016/j.yjmcc.2013.07.019 ↗
57. Combining cell and gene therapy to advance cardiac regeneration10.1080/14712598.2018.1430762 ↗
58. Functional screening identifies miRNAs inducing cardiac regeneration10.1038/nature11739 ↗
59. MicroRNAs and stem cells control of pluripotency, reprogramming, and lineage commitment10.1161/CIRCRESAHA.111.243394 ↗
60. Calcium upregulation by percutaneous administration of gene therapy in cardiac disease (CUPID) a phase 2 trial of intracoronary gene therapy of sarcoplasmic reticulum Ca2+-ATPase in patients with advanced heart failure10.1161/CIRCULATIONAHA.111.022889 ↗
61. Gene therapies in canine models for Duchenne muscular dystrophy10.1007/s00439-019-01976-z ↗
62. Systemic gene delivery clinical trial for Duchenne muscular dystrophy, ClinicalTrials.gov Identifier: NCT03375164, 2017. https://clinicaltrials.gov/ct2/show/NCT03375164?cond=%22Muscular+Dystrophy%2C++Duchenne%22&lupd_s=11%2F13%2F2015.
63. A study to evaluate the safety and tolerability of PF-06939926 gene therapy in Duchenne muscular dystrophy. https://clinicaltrials.gov/ct2/show/NCT03362502?cond=%22Muscular+Dystrophy%2C+.
64. DNA targeting specificity of RNA-guided Cas9 nucleases10.1038/nbt.2647 ↗