journal article·2022-11-16

Cell-Membrane-Coated Cationic Nanoparticles Disguised as Macrophages for the Prevention and Treatment of Type 2 Diabetes Mellitus

Lin Wu, Anran Yuan, Xiangrong Tian, Jin Cao, Xueyong Qi, Yuan Wei, Song Shen

ACS Applied Materials & Interfaces· Volume 14· Issue 45
Publisher page

Abstract

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disease characterized by low-grade inflammation and insulin resistance. In this process, innate immune cells play a crucial role in recognizing the stimuli (free fatty acid, lipopolysaccharide, and cytokines) and mediating the inflammatory response, contributing to the development of T2DM. Neutralizing inflammatory cytokines and blocking the inflammation cascade provide great potential for the treatment of T2DM. Here, we applied a macrophage membrane as a bait, which could specifically recognize and bind the stimuli, to encapsulate nanoparticles and capture the stimuli, further preventing inflammation. The in vivo experiment results suggest that the nanoparticles could reduce the production of proinflammatory cytokines, decrease insulin resistance, and realize significant therapeutic effects for T2DM. A potential strategy is thus offered for blocking immune response, holding a wide application in metabolic and autoimmune diseases.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Immune cells in cancer · Adipokines, Inflammation, and Metabolic Diseases · Tryptophan and brain disorders

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

Affiliations

Affiliated Hospital of Jiangsu University, Zhenjiang 212001, China

School of Pharmacy, Jiangsu University, Zhenjiang, Jiangsu 212013, China

Funding

National Natural Science Foundation of China

References (31)

Show source-provided references
1. 10.1038/nrendo.2015.18910.1038/nrendo.2015.189 ↗
2. 10.1038/nrd427510.1038/nrd4275 ↗
3. 10.1038/nri292510.1038/nri2925 ↗
4. 10.1111/j.1464-5491.2009.02847.x10.1111/j.1464-5491.2009.02847.x ↗
5. 10.2337/db06-149110.2337/db06-1491 ↗
6. 10.1016/j.metabol.2016.12.00910.1016/j.metabol.2016.12.009 ↗
7. 10.2337/db07-140310.2337/db07-1403 ↗
8. 10.1016/j.jsps.2015.03.01310.1016/j.jsps.2015.03.013 ↗
9. 10.1530/JME-15-023210.1530/JME-15-0232 ↗
10. 10.3390/nu1109202210.3390/nu11092022 ↗
11. 10.1038/nutd.2014.1010.1038/nutd.2014.10 ↗
12. 10.1038/ni77410.1038/ni774 ↗
13. 10.1016/j.biomaterials.2018.10.02910.1016/j.biomaterials.2018.10.029 ↗
14. 10.1021/acsami.8b0536310.1021/acsami.8b05363 ↗
15. 10.1021/acsnano.9b0277310.1021/acsnano.9b02773 ↗
16. 10.1038/s41565-018-0254-410.1038/s41565-018-0254-4 ↗
17. 10.1021/acsnano.8b0406610.1021/acsnano.8b04066 ↗
18. 10.1002/adma.20180223310.1002/adma.201802233 ↗
19. 10.1073/pnas.110663410810.1073/pnas.1106634108 ↗
20. 10.1038/srep3966110.1038/srep39661 ↗
21. 10.1021/acs.chemrev.6b0076510.1021/acs.chemrev.6b00765 ↗
22. 10.1038/cr.2013.8810.1038/cr.2013.88 ↗
23. 10.1073/pnas.130888711010.1073/pnas.1308887110 ↗
24. 10.1038/ncomms487810.1038/ncomms4878 ↗
25. 10.1038/nm.435010.1038/nm.4350 ↗
26. 10.1038/sj.jhh.100220110.1038/sj.jhh.1002201 ↗
27. 10.1371/journal.pone.016883910.1371/journal.pone.0168839 ↗
28. 10.1038/nnano.2012.21210.1038/nnano.2012.212 ↗
29. 10.1126/science.123072010.1126/science.1230720 ↗
30. 10.1016/j.foodchem.2011.02.04010.1016/j.foodchem.2011.02.040 ↗
31. 10.1016/j.ijbiomac.2016.05.03210.1016/j.ijbiomac.2016.05.032 ↗