pNiPAM-Nanoparticle-Based Antiapoptotic Approach for Pro-Regenerative Capacity of Skeletal Myogenic Cells

The biocompatibility of pNiPAM (Poly N-isopropylacrylamide) copolymers has been examined and they did not exert any cytotoxic effects. Their properties and vulnerable temperature characteristics make them candidates for use in medical applications. We synthesized a well-characterized nanoparticles-b...

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Main Authors: Magdalena Nowaczyk, Agnieszka Zimna, Tobiasz Deptuła, Katarzyna Fiedorowicz, Natalia Rozwadowska, Marta Podralska, Maciej Kurpisz
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/11/10/2495
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author Magdalena Nowaczyk
Agnieszka Zimna
Tobiasz Deptuła
Katarzyna Fiedorowicz
Natalia Rozwadowska
Marta Podralska
Maciej Kurpisz
author_facet Magdalena Nowaczyk
Agnieszka Zimna
Tobiasz Deptuła
Katarzyna Fiedorowicz
Natalia Rozwadowska
Marta Podralska
Maciej Kurpisz
author_sort Magdalena Nowaczyk
collection DOAJ
description The biocompatibility of pNiPAM (Poly N-isopropylacrylamide) copolymers has been examined and they did not exert any cytotoxic effects. Their properties and vulnerable temperature characteristics make them candidates for use in medical applications. We synthesized a well-characterized nanoparticles-based cargo system that would effectively deliver a biological agent to human skeletal myogenic cells (SkMCs); among other aspects, a downregulating apoptotic pathway potentially responsible for poor regeneration of myocardium. We confirmed the size of the pNiPAM based spheres at around 100 nm and the nanomeric shape of nanoparticles (NP) obtained. We confirmed that 33 °C is the adequate temperature for phase transition. We performed the dynamics of cargo release. A small amount of examined protein was detected at 10 min after reaching LCTS (lower critical solution temperature). The presented results of the test with BSA (bovine serum albumin) and doxorubicin loaded into nanoparticles showed a similar release profile for both substances. SkMCs incubated with NP loaded with antiapoptotic agent, BCB (Bax channel blocker), significantly diminished cell apoptosis (<i>p</i> < 0.01). Moreover, the lowest apoptotic level was detected in SkMCs treated with camptothecin and simultaneously incubated with pNiPAMs loaded with BCB. Application of nanoparticles loaded with BCB or subjected to BCB alone did not, however, diminish the amount of apparently necrotic cells.
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spelling doaj.art-4418787b688c427c94ccd9d4e5c8827a2023-11-22T19:22:08ZengMDPI AGNanomaterials2079-49912021-09-011110249510.3390/nano11102495pNiPAM-Nanoparticle-Based Antiapoptotic Approach for Pro-Regenerative Capacity of Skeletal Myogenic CellsMagdalena Nowaczyk0Agnieszka Zimna1Tobiasz Deptuła2Katarzyna Fiedorowicz3Natalia Rozwadowska4Marta Podralska5Maciej Kurpisz6Institute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, PolandInstitute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, PolandInstitute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, PolandInstitute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, PolandInstitute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, PolandInstitute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, PolandInstitute of Human Genetics, Polish Academy of Sciences, 60-479 Poznan, PolandThe biocompatibility of pNiPAM (Poly N-isopropylacrylamide) copolymers has been examined and they did not exert any cytotoxic effects. Their properties and vulnerable temperature characteristics make them candidates for use in medical applications. We synthesized a well-characterized nanoparticles-based cargo system that would effectively deliver a biological agent to human skeletal myogenic cells (SkMCs); among other aspects, a downregulating apoptotic pathway potentially responsible for poor regeneration of myocardium. We confirmed the size of the pNiPAM based spheres at around 100 nm and the nanomeric shape of nanoparticles (NP) obtained. We confirmed that 33 °C is the adequate temperature for phase transition. We performed the dynamics of cargo release. A small amount of examined protein was detected at 10 min after reaching LCTS (lower critical solution temperature). The presented results of the test with BSA (bovine serum albumin) and doxorubicin loaded into nanoparticles showed a similar release profile for both substances. SkMCs incubated with NP loaded with antiapoptotic agent, BCB (Bax channel blocker), significantly diminished cell apoptosis (<i>p</i> < 0.01). Moreover, the lowest apoptotic level was detected in SkMCs treated with camptothecin and simultaneously incubated with pNiPAMs loaded with BCB. Application of nanoparticles loaded with BCB or subjected to BCB alone did not, however, diminish the amount of apparently necrotic cells.https://www.mdpi.com/2079-4991/11/10/2495nanoparticlespNiPAMapoptosisnecrosisbax channel blockerskeletal muscle derived stem/progenitor cells
spellingShingle Magdalena Nowaczyk
Agnieszka Zimna
Tobiasz Deptuła
Katarzyna Fiedorowicz
Natalia Rozwadowska
Marta Podralska
Maciej Kurpisz
pNiPAM-Nanoparticle-Based Antiapoptotic Approach for Pro-Regenerative Capacity of Skeletal Myogenic Cells
Nanomaterials
nanoparticles
pNiPAM
apoptosis
necrosis
bax channel blocker
skeletal muscle derived stem/progenitor cells
title pNiPAM-Nanoparticle-Based Antiapoptotic Approach for Pro-Regenerative Capacity of Skeletal Myogenic Cells
title_full pNiPAM-Nanoparticle-Based Antiapoptotic Approach for Pro-Regenerative Capacity of Skeletal Myogenic Cells
title_fullStr pNiPAM-Nanoparticle-Based Antiapoptotic Approach for Pro-Regenerative Capacity of Skeletal Myogenic Cells
title_full_unstemmed pNiPAM-Nanoparticle-Based Antiapoptotic Approach for Pro-Regenerative Capacity of Skeletal Myogenic Cells
title_short pNiPAM-Nanoparticle-Based Antiapoptotic Approach for Pro-Regenerative Capacity of Skeletal Myogenic Cells
title_sort pnipam nanoparticle based antiapoptotic approach for pro regenerative capacity of skeletal myogenic cells
topic nanoparticles
pNiPAM
apoptosis
necrosis
bax channel blocker
skeletal muscle derived stem/progenitor cells
url https://www.mdpi.com/2079-4991/11/10/2495
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