4.5 Article

THE NUCLEUS PULPOSUS MICROENVIRONMENT IN THE INTERVERTEBRAL DISC: THE FOUNTAIN OF YOUTH?

期刊

EUROPEAN CELLS & MATERIALS
卷 41, 期 -, 页码 707-738

出版社

AO RESEARCH INSTITUTE DAVOS-ARI
DOI: 10.22203/eCM.v041a46

关键词

Tissue engineering; regenerative medicine; intervertebral disc; nucleus pulposus; cell therapy; microenvironment; clinical research

资金

  1. H2020 project iPSpine [825925]
  2. Swiss National Science Project [310030E_192674/1]
  3. Swiss Society of Orthopaedics (SGOT)
  4. clinical trials unit of Bern, University Hospital Bern
  5. Eurospine Task Force Research grant [2019_22]
  6. Swiss National Science Foundation (SNF) [310030E_192674] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

Intervertebral disc degeneration remains a challenging issue for patients with limited treatment options. Understanding the components and interactions within the NP microenvironment is crucial for potential tissue engineering approaches and future clinical applications in promoting NP regeneration. Recent discoveries in NP tissue engineering related to the microenvironment highlight the importance of adjusting crosstalk within the microenvironment for successful outcomes in treating degenerative disc disease.
The intervertebral disc (IVD) is a complex tissue, and its degeneration remains a problem for patients, without significant improvement in treatment strategies. This mostly age-related disease predominantly affects the nucleus pulposus (NP), the central region of the IVD. The NP tissue, and especially its microenvironment, exhibit changes that may be involved at the outset or affect the progression of IVD pathology. The NP tissue microenvironment is unique and can be defined by a variety of specific factors and components characteristic of its physiology and function. NP progenitor cell interactions with their surrounding microenvironment may be a key factor for the regulation of cellular metabolism, phenotype, and stemness. Recently, cell-transplantation approaches have been investigated for the treatment of degenerative disc disease, highlighting the need to better understand if and how transplanted cells can give rise to healthy NP tissue. Hence, understanding all the components of the NP microenvironment seems to be critical to better gauge the success and outcomes of approaches for tissue engineering and future clinical applications. Knowledge about the components of the NP microenvironment, how NP progenitor cells interact with them, and how changes in their surroundings can alter their function is summarised. Recent discoveries in NP tissue engineering linked to the microenvironment are also reviewed, meaning how crosstalk within the microenvironment can be adjusted to promote NP regeneration. Associated clinical problems are also considered, connecting bench-to-bedside in the context of IVD degeneration.

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