Protein Coronas Derived from Mucus Act as Both Spear and Shield to Regulate Transferrin Functionalized Nanoparticle Transcellular Transport in Enterocytes
The epithelial mucosa is a key biological barrier faced by gastrointestinal, intraoral, intranasal, ocular, and vaginal drug delivery. Ligand-modified nanoparticles demonstrate excellent ability on this process, but their efficacy is diminished by the formation of protein coronas (PCs) when they interact with biological matrices. PCs are broadly implicated in affecting the fate of NPs in vivo and in vitro, yet few studies have investigated PCs formed during interactions of NPs with the epithelial mucosa, especially mucus. In this study, we constructed transferrin modified NPs (Tf-NPs) as a model and explored the mechanisms and effects that epithelial mucosa had on PCs formation and the subsequent impact on the transcellular transport of Tf-NPs. In mucus-secreting cells, Tf-NPs adsorbed more proteins from the mucus layers, which masked, displaced, and dampened the active targeting effects of Tf-NPs, thereby weakening endocytosis and transcellular transport efficiencies. In mucus-free cells, Tf-NPs adsorbed more proteins during intracellular trafficking, which enhanced transcytosis related functions. Inspired by soft coronas and artificial biomimetic membranes, we used mucin as an "active PC" to precoat Tf-NPs (MTf-NPs), which limited the negative impacts of "passive PCs" formed during interface with the epithelial mucosa and improved favorable routes of endocytosis. M@Tf-NPs adsorbed more proteins associated with endoplasmic reticulum-Golgi functions, prompting enhanced intracellular transport and exocytosis. In summary, mucus shielded against the absorption of Tf-NPs, but also could be employed as a spear to break through the epithelial mucosa barrier. These findings offer a theoretical foundation and design platform to enhance the efficiency of oral-administered nanomedicines.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:18 |
---|---|
Enthalten in: |
ACS nano - 18(2024), 10 vom: 12. März, Seite 7455-7472 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Yang, Dan [VerfasserIn] |
---|
Links: |
---|
Themen: |
Journal Article |
---|
Anmerkungen: |
Date Completed 13.03.2024 Date Revised 13.03.2024 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1021/acsnano.3c11315 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM369070801 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM369070801 | ||
003 | DE-627 | ||
005 | 20240313234523.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240229s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1021/acsnano.3c11315 |2 doi | |
028 | 5 | 2 | |a pubmed24n1326.xml |
035 | |a (DE-627)NLM369070801 | ||
035 | |a (NLM)38417159 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Yang, Dan |e verfasserin |4 aut | |
245 | 1 | 0 | |a Protein Coronas Derived from Mucus Act as Both Spear and Shield to Regulate Transferrin Functionalized Nanoparticle Transcellular Transport in Enterocytes |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 13.03.2024 | ||
500 | |a Date Revised 13.03.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a The epithelial mucosa is a key biological barrier faced by gastrointestinal, intraoral, intranasal, ocular, and vaginal drug delivery. Ligand-modified nanoparticles demonstrate excellent ability on this process, but their efficacy is diminished by the formation of protein coronas (PCs) when they interact with biological matrices. PCs are broadly implicated in affecting the fate of NPs in vivo and in vitro, yet few studies have investigated PCs formed during interactions of NPs with the epithelial mucosa, especially mucus. In this study, we constructed transferrin modified NPs (Tf-NPs) as a model and explored the mechanisms and effects that epithelial mucosa had on PCs formation and the subsequent impact on the transcellular transport of Tf-NPs. In mucus-secreting cells, Tf-NPs adsorbed more proteins from the mucus layers, which masked, displaced, and dampened the active targeting effects of Tf-NPs, thereby weakening endocytosis and transcellular transport efficiencies. In mucus-free cells, Tf-NPs adsorbed more proteins during intracellular trafficking, which enhanced transcytosis related functions. Inspired by soft coronas and artificial biomimetic membranes, we used mucin as an "active PC" to precoat Tf-NPs (MTf-NPs), which limited the negative impacts of "passive PCs" formed during interface with the epithelial mucosa and improved favorable routes of endocytosis. M@Tf-NPs adsorbed more proteins associated with endoplasmic reticulum-Golgi functions, prompting enhanced intracellular transport and exocytosis. In summary, mucus shielded against the absorption of Tf-NPs, but also could be employed as a spear to break through the epithelial mucosa barrier. These findings offer a theoretical foundation and design platform to enhance the efficiency of oral-administered nanomedicines | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Transferrin-functionalized nanoparticles | |
650 | 4 | |a mucus | |
650 | 4 | |a nanobio interaction | |
650 | 4 | |a oral absorption | |
650 | 4 | |a protein corona | |
650 | 4 | |a protein-coated nanoparticles | |
650 | 7 | |a Protein Corona |2 NLM | |
650 | 7 | |a Transferrins |2 NLM | |
650 | 7 | |a Transferrin |2 NLM | |
700 | 1 | |a Feng, Yuqi |e verfasserin |4 aut | |
700 | 1 | |a Yuan, Ying |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Linxuan |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Yao |e verfasserin |4 aut | |
700 | 1 | |a Midgley, Adam C |e verfasserin |4 aut | |
700 | 1 | |a Wang, Yanrong |e verfasserin |4 aut | |
700 | 1 | |a Liu, Ning |e verfasserin |4 aut | |
700 | 1 | |a Li, Guoliang |e verfasserin |4 aut | |
700 | 1 | |a Yao, Xiaolin |e verfasserin |4 aut | |
700 | 1 | |a Liu, Dechun |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t ACS nano |d 2007 |g 18(2024), 10 vom: 12. März, Seite 7455-7472 |w (DE-627)NLM18248100X |x 1936-086X |7 nnns |
773 | 1 | 8 | |g volume:18 |g year:2024 |g number:10 |g day:12 |g month:03 |g pages:7455-7472 |
856 | 4 | 0 | |u http://dx.doi.org/10.1021/acsnano.3c11315 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 18 |j 2024 |e 10 |b 12 |c 03 |h 7455-7472 |