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      Notochordal Cell-Based Treatment Strategies and Their Potential in Intervertebral Disc Regeneration

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          Abstract

          Chronic low back pain is the number one cause of years lived with disability. In about 40% of patients, chronic lower back pain is related to intervertebral disc (IVD) degeneration. The standard-of-care focuses on symptomatic relief, while surgery is the last resort. Emerging therapeutic strategies target the underlying cause of IVD degeneration and increasingly focus on the relatively overlooked notochordal cells (NCs). NCs are derived from the notochord and once the notochord regresses they remain in the core of the developing IVD, the nucleus pulposus. The large vacuolated NCs rapidly decline after birth and are replaced by the smaller nucleus pulposus cells with maturation, ageing, and degeneration. Here, we provide an update on the journey of NCs and discuss the cell markers and tools that can be used to study their fate and regenerative capacity. We review the therapeutic potential of NCs for the treatment of IVD-related lower back pain and outline important future directions in this area. Promising studies indicate that NCs and their secretome exerts regenerative effects, via increased proliferation, extracellular matrix production, and anti-inflammatory effects. Reports on NC-like cells derived from embryonic- or induced pluripotent-stem cells claim to have successfully generated NC-like cells but did not compare them with native NCs for phenotypic markers or in terms of their regenerative capacity. Altogether, this is an emerging and active field of research with exciting possibilities. NC-based studies demonstrate that cues from developmental biology can pave the path for future clinical therapies focused on regenerating the diseased IVD.

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          Most cited references203

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          Global low back pain prevalence and years lived with disability from 1990 to 2017: estimates from the Global Burden of Disease Study 2017

          Background Low back pain (LBP) is a common musculoskeletal problem globally. Updating the prevalence and burden of LBP is important for researchers and policy makers. This paper presents, compares and contextualizes the global prevalence and years lived with disability (YLDs) of LBP by age, sex and region, from 1990 to 2017. Methods Data were extracted from the GBD (the Global Burden of Disease, Injuries, and Risk Factors Study) 2017 Study. Age, sex and region-specific analyses were conducted to estimate the global prevalence and YLDs of LBP, with the uncertainty intervals (UIs). Results The age-standardized point prevalence of LBP was 8.20% (95% UI: 7.31–9.10%) in 1990 and decreased slightly to 7.50% (95% UI: 6.75–8.27%) in 2017. The prevalent numbers of people with LBP at any one point in time in 1990 was 377.5 million, and this increased to 577.0 million in 2017. Age-standardized prevalence of LBP was higher in females than males. LBP prevalence increased with age, and peaked around the ages of 80 to 89 years, and then decreased slightly. Global YLDs were 42.5 million (95% UI: 30.2 million–57.2 million) in 1990 and increased by 52.7% to 64.9 million (95% UI: 46.5 million–87.4 million) in 2017. YLDs were also higher in females than males and increased initially with age; they peaked at 35–39 years of age in 1990, before decreasing, whereas in 2017, they peaked at 45–49 years of age, before decreasing. Western Europe had the highest number of LBP YLDs. Conclusions Globally, LBP is the leading global cause of YLDs. Greater attention is urgently needed to mitigate this increasing burden and the impact it is having on health and social systems.
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            Low back pain in relation to lumbar disc degeneration.

            Cross-sectional magnetic resonance imaging (MRI) study. To study the relation of low back pain (LBP) to disc degeneration in the lumbar spine. Controversy still prevails about the relationship between disc degeneration and LBP. Classification of disc degeneration and symptoms varies, hampering comparison of study results. Subjects comprised 164 men aged 40-45 years-53 machine drivers, 51 construction carpenters, and 60 office workers. The data of different types of LBP, individual characteristics, and lifestyle factors were obtained from a questionnaire and a structured interview. Degeneration of discs L2/L3-L5/S1 (dark nucleus pulposus and posterior and anterior bulge) was assessed with MRI. An increased risk of LBP (including all types) was found in relation to all signs of disc degeneration. An increased risk of sciatic pain was found in relation to posterior bulges, but local LBP was not related to disc degeneration. The risks of LBP and sciatic pain were strongly affected by occupation. Low back pain is associated with signs of disc degeneration and sciatic pain with posterior disc bulges. Low back pain is strongly associated with occupation.
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              Cells respond to mechanical stress by rapid disassembly of caveolae.

              The functions of caveolae, the characteristic plasma membrane invaginations, remain debated. Their abundance in cells experiencing mechanical stress led us to investigate their role in membrane-mediated mechanical response. Acute mechanical stress induced by osmotic swelling or by uniaxial stretching results in a rapid disappearance of caveolae, in a reduced caveolin/Cavin1 interaction, and in an increase of free caveolins at the plasma membrane. Tether-pulling force measurements in cells and in plasma membrane spheres demonstrate that caveola flattening and disassembly is the primary actin- and ATP-independent cell response that buffers membrane tension surges during mechanical stress. Conversely, stress release leads to complete caveola reassembly in an actin- and ATP-dependent process. The absence of a functional caveola reservoir in myotubes from muscular dystrophic patients enhanced membrane fragility under mechanical stress. Our findings support a new role for caveolae as a physiological membrane reservoir that quickly accommodates sudden and acute mechanical stresses. Copyright © 2011 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Front Cell Dev Biol
                Front Cell Dev Biol
                Front. Cell Dev. Biol.
                Frontiers in Cell and Developmental Biology
                Frontiers Media S.A.
                2296-634X
                14 March 2022
                2021
                : 9
                : 780749
                Affiliations
                [1] 1 Department of Clinical Sciences , Faculty of Veterinary Medicine , Utrecht University , Utrecht, Netherlands
                [2] 2 UMR 1229-RMeS , Regenerative Medicine and Skeleton , Université de Nantes , ONIRIS , Nantes, France
                [3] 3 UFR Odontologie , Université de Nantes , Nantes, France
                [4] 4 PHU4 OTONN , CHU Nantes , Nantes, France
                [5] 5 Leni and Peter W. May Department of Orthopaedics , Icahn School of Medicine at Mount Sinai , New York, NY, United States
                [6] 6 School of Biomedical Sciences , The University of Hong Kong , Hong Kong SAR, China
                [7] 7 Orthopaedic Biomechanics , Department of Biomedical Engineering , Eindhoven University of Technology , Eindhoven, Netherlands
                [8] 8 Department of Orthopedics , University Medical Centre Utrecht , Utrecht, Netherlands
                [9] 9 Biomolecular Sciences Research Centre , Sheffield Hallam University , Sheffield, United Kingdom
                Author notes

                Edited by: Bo Gao, Air Force Military Medical University, China

                Reviewed by: Jianquan Chen, Soochow University, China

                Jeroen Geurts, University of Lausanne, Switzerland

                *Correspondence: Marianna A. Tryfonidou, m.a.tryfonidou@ 123456uu.nl

                This article was submitted to Molecular and Cellular Pathology, a section of the journal Frontiers in Cell and Developmental Biology

                Article
                780749
                10.3389/fcell.2021.780749
                8963872
                35359916
                85a13fa4-222a-4d63-9e1c-0c2a0e44519c
                Copyright © 2022 Bach, Poramba-Liyanage, Riemers, Guicheux, Camus, Iatridis, Chan, Ito, Le Maitre and Tryfonidou.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 21 September 2021
                : 15 November 2021
                Funding
                Funded by: Horizon 2020 Framework Programme , doi 10.13039/100010661;
                Funded by: Agence Nationale de la Recherche , doi 10.13039/501100001665;
                Funded by: Fondation pour la Recherche Médicale , doi 10.13039/501100002915;
                Funded by: AO Foundation , doi 10.13039/501100001702;
                Funded by: Dutch Arthritis Society , doi 10.13039/100018286;
                Funded by: Research Grants Council, University Grants Committee , doi 10.13039/501100002920;
                Categories
                Cell and Developmental Biology
                Review

                intervertebral disc – degeneration,conditioned media (cm),secretome,low back pain,extracellular matrix (ecm),cell therapeutic potential,notochordal cell

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