Table 1.
Cell-Derived Nanocarriers | Surface Markers | Size | Source Cell | Loading Strategies |
mRNA Cargos |
Target Strategies |
Application | Ref. |
---|---|---|---|---|---|---|---|---|
Exosomes | TSG101 and CD9 | 50–200 nm | 293T | Passive loading | Luciferase or PGC1α | miRNA-dependent mRNA expression and ultrasound | Obesity | [44] |
Exosomes | CD9, TSG101, and CD63 | 30–160 nm | 293T | Passive loading | Bmp7 | Ultrasound | Obesity | [45] |
MVs | NA | Mostly 100–150 nm | HEK-293T | Passive loading | CD-UPRT-EGFP | Prodrug | Schwannoma tumor | [46] |
Exosomes | TSG101 and CD9 | 50–200 nm | HEK293T | Passive loading | Il-10 | miRNA- dependent mRNA expression | Inflammation of atherosclerosis | [47] |
Exosomes | Lamp2b, CD63, Alix, and Tsg101 | 20–500 nm | HEK293 | Passive loading | Nerve growth factor | RVG-Lamp2b | Cerebral ischemia | [48] |
Exosomes | CD9, CD63, CD47, and Tsg101 | NA | MEFs and DCs | Passive loading based on a cellular nanoporation system | PTEN | Fuse glioma-targeting peptides to CD47 | Glioma tumor | [49] |
Exosomes | CD9, TSG101 | 30–150 nm | AML12 | Passive loading | Ldlr | NA | Familial hypercholesterolemia | [50] |
Exosomes | CD63, Lamp2b, CD9 and TSG101 | 50–200 nm | HEK-293T | Active loading based on L7Ae-CD63 fusion protein | nluc or catalase | RVG-Lamp2b | Parkinson’s disease | [51] |
Exosomes | Lamp2b and CD63 | 50–200 nm | 293FT | TAMEL platform | DTomato or Cas9 | NA | NA | [52] |
Exosomes | CD63, CD9, and TSG101 | 100–200 nm | 293T | Active loading based on CD9-HUR fusion protein | Cas9 | NA | NA | [53] |
Exosomes | CD9 and Lamp2b | 100–300 nm | 293T | Active loading based on a specific DNA aptamer | GFP, PGC1α or Il-10 | ATS-Lamp2b | Obesity and intestinal inflammation |
[54] |
Exosomes | CD63, Alix, and TSG101 | Average ~100 nm | HEK293T | Active loading based on L7Ae-CD63 fusion protein | ZPAMt | NA | HIV-1 infection | [55] |
Exosomes | CD63, CD81, and lactadherin | 30–100 nm; | HEK293 | Active loading based on EV-loading zipcode sequence | HChrR6 | Prodrug | HER2 + ve human breast cancer | [56] |
MVs | ARRDC1 | <100 nm | 293T | Active loading based on Tat-ARRDC1 fusion protein | GFP or p53 | NA | NA | [57] |
Outer membrane vesicles | ClyA | average 28.1 nm | BL21 (DE3) Escherichia coli | Active loading based on ClyA-L7Ae fusion protein | EGFP, OVA or ADPGK | NA | Melanoma and colon cancer | [58] |
Exosomes | Glycophorin A, ALIX, and TSG1–1 | 120–200 nm | Red blood cells | Post-loading based on REG1 loading reagent | Luciferase | An enzymatic method | NA | [59] |
A mixture of exosomes and MVs | ALIX, TSG101, hemoglobin A, and Stomatin | 100–300 nm (average ~140 nm) | Red blood cells | Post-loading based on electroporation | Cas9 | NA | NA | [60] |
Exosomes | CD63 | ~110 nm | HEK293T or lung spheroid cells | Post-loading based on electroporation | GFP | NA | NA | [61] |
Exosomes | NA | ~200 nm | HEK293T or lung spheroid cells | Post-loading based on electroporation | GFP or SARS-CoV-2 spike protein | NA | COVID-19 | [62] |
Cell membrane-coated PLGA NPs | NA | average 185 nm | B16F10 | Double emulsion method with the assistance of G0-C14 | EGFP or Cypridina luciferase | NA | NA | [43] |
MEFs, mouse embryonic fibroblasts; DCs, dendritic cells; HUR, human antigen R; ARRDC1, arrestin domain containing protein; Cas9, CRISPR-associated protein 9; GFP, green fluorescent protein; nluc, NanoLuc luciferase; EGFP, enhanced green fluorescent protein; OVA, ovalbumin; Ldlr, low density lipoprotein receptor; RVG, rabies viral glycoprotein. PTEN, a tumor suppressor phosphatase and tensin homolog deleted on chromosome 10; Lamp2b, lysosome-associated membrane protein 2; SARS-CoV-2, severe acute respiratory coronavirus 2; COVID-19, coronavirus disease 2019; NA, not applicable.