Cargando…

Injectable Cell-Laden Nanofibrous Matrix for Treating Annulus Fibrosus Defects in Porcine Model: An Organ Culture Study

Lower back pain commonly arises from intervertebral disc (IVD) failure, often caused by deteriorating annulus fibrosus (AF) and/or nucleus pulposus (NP) tissue. High socioeconomic cost, quality of life issues, and unsatisfactory surgical options motivate the rapid development of non-invasive, regene...

Descripción completa

Detalles Bibliográficos
Autores principales: Roebke, Evan, Jacho, Diego, Eby, Oliver, Aldoohan, Sulaiman, Elsamaloty, Haitham, Yildirim-Ayan, Eda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694927/
https://www.ncbi.nlm.nih.gov/pubmed/36431001
http://dx.doi.org/10.3390/life12111866
_version_ 1784837928275410944
author Roebke, Evan
Jacho, Diego
Eby, Oliver
Aldoohan, Sulaiman
Elsamaloty, Haitham
Yildirim-Ayan, Eda
author_facet Roebke, Evan
Jacho, Diego
Eby, Oliver
Aldoohan, Sulaiman
Elsamaloty, Haitham
Yildirim-Ayan, Eda
author_sort Roebke, Evan
collection PubMed
description Lower back pain commonly arises from intervertebral disc (IVD) failure, often caused by deteriorating annulus fibrosus (AF) and/or nucleus pulposus (NP) tissue. High socioeconomic cost, quality of life issues, and unsatisfactory surgical options motivate the rapid development of non-invasive, regenerative repair strategies for lower back pain. This study aims to evaluate the AF regenerative capacity of injectable matrix repair strategy in ex vivo porcine organ culturing using collagen type-I and polycaprolactone nanofibers (PNCOL) with encapsulated fibroblast cells. Upon 14 days organ culturing, the porcine IVDs were assessed using gross optical imaging, magnetic resonance imaging (MRI), histological analysis, and Reverse Transcriptase quantitative PCR (RT-qPCR) to determine the regenerative capabilities of the PNCOL matrix at the AF injury. PNCOL-treated AF defects demonstrated a full recovery with increased gene expressions of AF extracellular matrix markers, including Collagen-I, Aggrecan, Scleraxis, and Tenascin, along with anti-inflammatory markers such as CD206 and IL10. The PNCOL treatment effectively regenerates the AF tissue at the injury site contributing to decreased herniation risk and improved surgical outcomes, thus providing effective non-invasive strategies for treating IVD injuries.
format Online
Article
Text
id pubmed-9694927
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96949272022-11-26 Injectable Cell-Laden Nanofibrous Matrix for Treating Annulus Fibrosus Defects in Porcine Model: An Organ Culture Study Roebke, Evan Jacho, Diego Eby, Oliver Aldoohan, Sulaiman Elsamaloty, Haitham Yildirim-Ayan, Eda Life (Basel) Article Lower back pain commonly arises from intervertebral disc (IVD) failure, often caused by deteriorating annulus fibrosus (AF) and/or nucleus pulposus (NP) tissue. High socioeconomic cost, quality of life issues, and unsatisfactory surgical options motivate the rapid development of non-invasive, regenerative repair strategies for lower back pain. This study aims to evaluate the AF regenerative capacity of injectable matrix repair strategy in ex vivo porcine organ culturing using collagen type-I and polycaprolactone nanofibers (PNCOL) with encapsulated fibroblast cells. Upon 14 days organ culturing, the porcine IVDs were assessed using gross optical imaging, magnetic resonance imaging (MRI), histological analysis, and Reverse Transcriptase quantitative PCR (RT-qPCR) to determine the regenerative capabilities of the PNCOL matrix at the AF injury. PNCOL-treated AF defects demonstrated a full recovery with increased gene expressions of AF extracellular matrix markers, including Collagen-I, Aggrecan, Scleraxis, and Tenascin, along with anti-inflammatory markers such as CD206 and IL10. The PNCOL treatment effectively regenerates the AF tissue at the injury site contributing to decreased herniation risk and improved surgical outcomes, thus providing effective non-invasive strategies for treating IVD injuries. MDPI 2022-11-12 /pmc/articles/PMC9694927/ /pubmed/36431001 http://dx.doi.org/10.3390/life12111866 Text en © 2022 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
Roebke, Evan
Jacho, Diego
Eby, Oliver
Aldoohan, Sulaiman
Elsamaloty, Haitham
Yildirim-Ayan, Eda
Injectable Cell-Laden Nanofibrous Matrix for Treating Annulus Fibrosus Defects in Porcine Model: An Organ Culture Study
title Injectable Cell-Laden Nanofibrous Matrix for Treating Annulus Fibrosus Defects in Porcine Model: An Organ Culture Study
title_full Injectable Cell-Laden Nanofibrous Matrix for Treating Annulus Fibrosus Defects in Porcine Model: An Organ Culture Study
title_fullStr Injectable Cell-Laden Nanofibrous Matrix for Treating Annulus Fibrosus Defects in Porcine Model: An Organ Culture Study
title_full_unstemmed Injectable Cell-Laden Nanofibrous Matrix for Treating Annulus Fibrosus Defects in Porcine Model: An Organ Culture Study
title_short Injectable Cell-Laden Nanofibrous Matrix for Treating Annulus Fibrosus Defects in Porcine Model: An Organ Culture Study
title_sort injectable cell-laden nanofibrous matrix for treating annulus fibrosus defects in porcine model: an organ culture study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694927/
https://www.ncbi.nlm.nih.gov/pubmed/36431001
http://dx.doi.org/10.3390/life12111866
work_keys_str_mv AT roebkeevan injectablecellladennanofibrousmatrixfortreatingannulusfibrosusdefectsinporcinemodelanorganculturestudy
AT jachodiego injectablecellladennanofibrousmatrixfortreatingannulusfibrosusdefectsinporcinemodelanorganculturestudy
AT ebyoliver injectablecellladennanofibrousmatrixfortreatingannulusfibrosusdefectsinporcinemodelanorganculturestudy
AT aldoohansulaiman injectablecellladennanofibrousmatrixfortreatingannulusfibrosusdefectsinporcinemodelanorganculturestudy
AT elsamalotyhaitham injectablecellladennanofibrousmatrixfortreatingannulusfibrosusdefectsinporcinemodelanorganculturestudy
AT yildirimayaneda injectablecellladennanofibrousmatrixfortreatingannulusfibrosusdefectsinporcinemodelanorganculturestudy