Literature DB >> 27474175

Featured Article: Nanoenhanced matrix metalloproteinase-responsive delivery vehicles for disease resolution and imaging.

Donald A McCarthy1, Ahmad A Nazem1, James McNeilan1, Nicole L Shakerley1, Ryan R Clark1, María D Idelchik1, Mehmet Yigit2, J Andrés Melendez1.   

Abstract

The wide array of proteases, including matrix metalloproteinases, produced in response to many pathogenic insults, confers a unique proteolytic signature which is often disease specific and provides a potential therapeutic target for drug delivery. Here we propose the use of collagen-based nanoenhanced matrix metalloproteinase-responsive delivery vehicles that display matrix metalloproteinase-specific degradation in diverse in vitro models of proteolysis. We demonstrate that collagen particles comprised of protease substrates (primarily collagen) can be made of uniform size and loaded efficiently with assorted cargo including fluorescently labeled mesoporous silica, magnetic nanoparticles, proteins and antioxidants. We also demonstrate that pathologic concentrations of proteases produced in situ or in vitro display protease-specific cargo release. Additionally, we show that the collagen-based particles display bright fluorescence when loaded with a fluorophore, and have the potential to be used as vehicles for targeted delivery of drugs or imaging agents to regions of high proteolytic activity.

Entities:  

Keywords:  Collagen; antioxidants; burn injury; infection; matrix metalloproteinase; nanoparticles; proteases; senescence

Mesh:

Substances:

Year:  2016        PMID: 27474175      PMCID: PMC5102141          DOI: 10.1177/1535370216662534

Source DB:  PubMed          Journal:  Exp Biol Med (Maywood)        ISSN: 1535-3699


  41 in total

1.  Glucocorticoids suppress selected components of the senescence-associated secretory phenotype.

Authors:  Remi-Martin Laberge; Lili Zhou; Melissa R Sarantos; Francis Rodier; Adam Freund; Peter L J de Keizer; Su Liu; Marco Demaria; Yu-Sheng Cong; Pankaj Kapahi; Pierre-Yves Desprez; Robert E Hughes; Judith Campisi
Journal:  Aging Cell       Date:  2012-04-17       Impact factor: 9.304

2.  Reactive oxygen species control senescence-associated matrix metalloproteinase-1 through c-Jun-N-terminal kinase.

Authors:  Jaya Dasgupta; Supriya Kar; Rong Liu; Joy Joseph; Balaraman Kalyanaraman; S James Remington; Ceshi Chen; J Andres Melendez
Journal:  J Cell Physiol       Date:  2010-10       Impact factor: 6.384

3.  p38MAPK is a novel DNA damage response-independent regulator of the senescence-associated secretory phenotype.

Authors:  Adam Freund; Christopher K Patil; Judith Campisi
Journal:  EMBO J       Date:  2011-03-11       Impact factor: 11.598

4.  Redox-dependent matrix metalloproteinase-1 expression is regulated by JNK through Ets and AP-1 promoter motifs.

Authors:  Kristin K Nelson; Sita Subbaram; Kip M Connor; Jaya Dasgupta; Xiao-Fang Ha; Tzu-Ching Meng; Nicholas K Tonks; J Andres Melendez
Journal:  J Biol Chem       Date:  2006-03-28       Impact factor: 5.157

5.  Novel mutant green fluorescent protein protease substrates reveal the activation of specific caspases during apoptosis.

Authors:  N P Mahajan; D C Harrison-Shostak; J Michaux; B Herman
Journal:  Chem Biol       Date:  1999-06

6.  Senescence-associated genes in normal human oral keratinocytes.

Authors:  Mo K Kang; Ayako Kameta; Ki-Hyuk Shin; Marcel A Baluda; Hae-Ryun Kim; No-Hee Park
Journal:  Exp Cell Res       Date:  2003-07-15       Impact factor: 3.905

7.  Biochemical characterization of human collagenase-3.

Authors:  V Knäuper; C López-Otin; B Smith; G Knight; G Murphy
Journal:  J Biol Chem       Date:  1996-01-19       Impact factor: 5.157

Review 8.  Collagen structure and stability.

Authors:  Matthew D Shoulders; Ronald T Raines
Journal:  Annu Rev Biochem       Date:  2009       Impact factor: 23.643

Review 9.  Proteases in cancer drug delivery.

Authors:  Jennifer Vandooren; Ghislain Opdenakker; Paul M Loadman; Dylan R Edwards
Journal:  Adv Drug Deliv Rev       Date:  2016-01-03       Impact factor: 15.470

10.  Naturally occurring p16(Ink4a)-positive cells shorten healthy lifespan.

Authors:  Darren J Baker; Bennett G Childs; Matej Durik; Melinde E Wijers; Cynthia J Sieben; Jian Zhong; Rachel A Saltness; Karthik B Jeganathan; Grace Casaclang Verzosa; Abdulmohammad Pezeshki; Khashayarsha Khazaie; Jordan D Miller; Jan M van Deursen
Journal:  Nature       Date:  2016-02-03       Impact factor: 49.962

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.