Cargando…

Microfluidic Chip with Low Constant-Current Stimulation (LCCS) Platform: Human Nucleus Pulposus Degeneration In Vitro Model for Symptomatic Intervertebral Disc

Intervertebral disc (IVD) degeneration is a major cause of low back pain (LBP) in the lumbar spine. This phenomenon is caused by several processes, including matrix degradation in IVD tissues, which is mediated by matrix metalloproteinases (MMPs) and inflammatory responses, which can be mediated by...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, An-Gi, Kim, Tae-Won, Kwon, Woo-Keun, Lee, Kwang-Ho, Jeong, Sehoon, Hwang, Min-Ho, Choi, Hyuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621874/
https://www.ncbi.nlm.nih.gov/pubmed/34832700
http://dx.doi.org/10.3390/mi12111291
_version_ 1784605560027480064
author Kim, An-Gi
Kim, Tae-Won
Kwon, Woo-Keun
Lee, Kwang-Ho
Jeong, Sehoon
Hwang, Min-Ho
Choi, Hyuk
author_facet Kim, An-Gi
Kim, Tae-Won
Kwon, Woo-Keun
Lee, Kwang-Ho
Jeong, Sehoon
Hwang, Min-Ho
Choi, Hyuk
author_sort Kim, An-Gi
collection PubMed
description Intervertebral disc (IVD) degeneration is a major cause of low back pain (LBP) in the lumbar spine. This phenomenon is caused by several processes, including matrix degradation in IVD tissues, which is mediated by matrix metalloproteinases (MMPs) and inflammatory responses, which can be mediated by interactions among immune cells, such as macrophages and IVD cells. In particular, interleukin (IL)-1 beta (β), which is a master regulator secreted by macrophages, mediates the inflammatory response in nucleus pulposus cells (NP) and plays a significant role in the development or progression of diseases. In this study, we developed a custom electrical stimulation (ES) platform that can apply low-constant-current stimulation (LCCS) signals to microfluidic chips. Using this platform, we examined the effects of LCCS on IL-1β-mediated inflammatory NP cells, administered at various currents (5, 10, 20, 50, and 100 μA at 200 Hz). Our results showed that the inflammatory response, induced by IL-1β in human NP cells, was successfully established. Furthermore, 5, 10, 20, and 100 μA LCCS positively modulated inflamed human NP cells’ morphological phenotype and kinetic properties. LCCS could affect the treatment of degenerative diseases, revealing the applicability of the LCCS platform for basic research of electroceuticals.
format Online
Article
Text
id pubmed-8621874
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86218742021-11-27 Microfluidic Chip with Low Constant-Current Stimulation (LCCS) Platform: Human Nucleus Pulposus Degeneration In Vitro Model for Symptomatic Intervertebral Disc Kim, An-Gi Kim, Tae-Won Kwon, Woo-Keun Lee, Kwang-Ho Jeong, Sehoon Hwang, Min-Ho Choi, Hyuk Micromachines (Basel) Article Intervertebral disc (IVD) degeneration is a major cause of low back pain (LBP) in the lumbar spine. This phenomenon is caused by several processes, including matrix degradation in IVD tissues, which is mediated by matrix metalloproteinases (MMPs) and inflammatory responses, which can be mediated by interactions among immune cells, such as macrophages and IVD cells. In particular, interleukin (IL)-1 beta (β), which is a master regulator secreted by macrophages, mediates the inflammatory response in nucleus pulposus cells (NP) and plays a significant role in the development or progression of diseases. In this study, we developed a custom electrical stimulation (ES) platform that can apply low-constant-current stimulation (LCCS) signals to microfluidic chips. Using this platform, we examined the effects of LCCS on IL-1β-mediated inflammatory NP cells, administered at various currents (5, 10, 20, 50, and 100 μA at 200 Hz). Our results showed that the inflammatory response, induced by IL-1β in human NP cells, was successfully established. Furthermore, 5, 10, 20, and 100 μA LCCS positively modulated inflamed human NP cells’ morphological phenotype and kinetic properties. LCCS could affect the treatment of degenerative diseases, revealing the applicability of the LCCS platform for basic research of electroceuticals. MDPI 2021-10-21 /pmc/articles/PMC8621874/ /pubmed/34832700 http://dx.doi.org/10.3390/mi12111291 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, An-Gi
Kim, Tae-Won
Kwon, Woo-Keun
Lee, Kwang-Ho
Jeong, Sehoon
Hwang, Min-Ho
Choi, Hyuk
Microfluidic Chip with Low Constant-Current Stimulation (LCCS) Platform: Human Nucleus Pulposus Degeneration In Vitro Model for Symptomatic Intervertebral Disc
title Microfluidic Chip with Low Constant-Current Stimulation (LCCS) Platform: Human Nucleus Pulposus Degeneration In Vitro Model for Symptomatic Intervertebral Disc
title_full Microfluidic Chip with Low Constant-Current Stimulation (LCCS) Platform: Human Nucleus Pulposus Degeneration In Vitro Model for Symptomatic Intervertebral Disc
title_fullStr Microfluidic Chip with Low Constant-Current Stimulation (LCCS) Platform: Human Nucleus Pulposus Degeneration In Vitro Model for Symptomatic Intervertebral Disc
title_full_unstemmed Microfluidic Chip with Low Constant-Current Stimulation (LCCS) Platform: Human Nucleus Pulposus Degeneration In Vitro Model for Symptomatic Intervertebral Disc
title_short Microfluidic Chip with Low Constant-Current Stimulation (LCCS) Platform: Human Nucleus Pulposus Degeneration In Vitro Model for Symptomatic Intervertebral Disc
title_sort microfluidic chip with low constant-current stimulation (lccs) platform: human nucleus pulposus degeneration in vitro model for symptomatic intervertebral disc
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621874/
https://www.ncbi.nlm.nih.gov/pubmed/34832700
http://dx.doi.org/10.3390/mi12111291
work_keys_str_mv AT kimangi microfluidicchipwithlowconstantcurrentstimulationlccsplatformhumannucleuspulposusdegenerationinvitromodelforsymptomaticintervertebraldisc
AT kimtaewon microfluidicchipwithlowconstantcurrentstimulationlccsplatformhumannucleuspulposusdegenerationinvitromodelforsymptomaticintervertebraldisc
AT kwonwookeun microfluidicchipwithlowconstantcurrentstimulationlccsplatformhumannucleuspulposusdegenerationinvitromodelforsymptomaticintervertebraldisc
AT leekwangho microfluidicchipwithlowconstantcurrentstimulationlccsplatformhumannucleuspulposusdegenerationinvitromodelforsymptomaticintervertebraldisc
AT jeongsehoon microfluidicchipwithlowconstantcurrentstimulationlccsplatformhumannucleuspulposusdegenerationinvitromodelforsymptomaticintervertebraldisc
AT hwangminho microfluidicchipwithlowconstantcurrentstimulationlccsplatformhumannucleuspulposusdegenerationinvitromodelforsymptomaticintervertebraldisc
AT choihyuk microfluidicchipwithlowconstantcurrentstimulationlccsplatformhumannucleuspulposusdegenerationinvitromodelforsymptomaticintervertebraldisc