Cited by 1,708Bone Tissue Engineering MaterialsTissue Engineering and Regenerative MedicineSpine and Intervertebral Disc Pathology

Scaffolding in tissue engineering: general approaches and tissue-specific considerations

Open access
Chan, B. P., Leong, K. W.·2008·European Spine Journal

Abstract

Scaffolds represent important components for tissue engineering. However, researchers often encounter an enormous variety of choices when selecting scaffolds for tissue engineering. This paper aims to review the functions of scaffolds and the major scaffolding approaches as important guidelines for selecting scaffolds and discuss the tissue-specific considerations for scaffolding, using intervertebral disc as an example.

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Crossref · 10.1007/s00586-008-0745-3

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134 of 134 references verified0 citation errors · 0 not checkable

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  • dLECM preserves the complex network of collagen, fibronectin, growth factors, and other bioactive molecules, keeping the biological blueprint of the liver intact.

    “By stripping away cells while preserving the complex network of collagen, fibronectin, growth factors, and other bioactive molecules, dLECM keeps the “biological blueprint” of the liver intact [6,7].”

    From From scaffold to function: A systematic review on dLECM-based hydrogels for liver tissue engineering — Fabrication, properties, and translational applications (2026) · cites this paper as [7]

    The 'Scaffolding approaches in tissue engineering' section says decellularization removes cellular components while preserving ECM components, and that growth factors may remain in the matrix. The 'Analogous functions of scaffolds and extracellular matrix' section describes collagen and fibronectin as ECM constituents or cues. Neither section establishes that decellularized liver ECM preserves those components specifically or keeps the liver’s biological blueprint intact; the paper also notes that decellularization must be optimized to minimize disturbance to ECM composition. (LLM, conf=0.86)

    Experimental — accuracy not yet measured

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Research works printed but not linked: 1

  1. [29]29. Coric D, Mummaneni PV (2008) Nucleus replacement tech- nologies. J Neurosurg Spine 8(2):115-120

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Authors
Chan, B. P., & Leong, K. W.
Affiliations
  • University of Hong Kong (HK)
  • Duke University (US)
Corresponding author
Chan, B. P.
Venue
European Spine Journal
Published
2008-11-13
Volume
17
Issue
S4
Pages
467-479
ISSN
  • 0940-6719 (ISSN-L)
  • 1432-0932
OpenAlex
W1974193257
Cited by
1,708
References
134
Citations by year
2026: 76 · 2025: 158 · 2024: 168 · 2023: 158 · 2022: 143 · 2021: 140 · 2020: 108 · 2019: 138 · 2018: 125 · 2017: 139 · 2016: 98 · 2015: 78 · 2014: 76 · 2013: 48 · 2012: 17
FWCI
0.85
Type
journal article
Language
en
Open access
Locations
  • European Spine Journal (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • The HKU Scholars Hub (University of Hong Kong) (submittedVersion)
Funders
  • Innovation and Technology Commission
  • Hong Kong Government
  • National Institutes of Health
  • National Institute of Biomedical Imaging and Bioengineering (R01EB003447, EB003447)
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Spine and Intervertebral Disc Pathology
Keywords
scaffolds, tissue engineering, intervertebral disc, cartilage regeneration
MeSH terms
Animals, Biocompatible Materials, Extracellular Matrix, Humans, Intervertebral Disc, Intervertebral Disc Displacement, Regeneration, Chondrocytes, Tissue Engineering, Intercellular Signaling Peptides and Proteins, Tissue Scaffolds

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