Cited by 1,008Wound Healing and TreatmentsConnective Tissue Growth Factor ResearchElectrospun Nanofibers in Biomedical Applications

The DOI matches its Crossref record, with a small difference in title or year; 194 of the 194 references it cites were found in a registry or an index.

Extracellular Matrix and Dermal Fibroblast Function in the Healing Wound

Open access
Tracy, Lauren E., Minasian, Raquel A., Caterson, E.J.·2016·Advances in Wound Care

Abstract

Significance: Fibroblasts play a critical role in normal wound healing. Various extracellular matrix (ECM) components, including collagens, fibrin, fibronectin, proteoglycans, glycosaminoglycans, and matricellular proteins, can be considered potent protagonists of fibroblast survival, migration, and metabolism. Recent Advances: Advances in tissue culture, tissue engineering, and ex vivo models have made the examination and precise measurements of ECM components in wound healing possible. Likewise, the development of specific transgenic animal models has created the opportunity to characterize the role of various ECM molecules in healing wounds. In addition, the recent characterization of new ECM molecules, including matricellular proteins, dermatopontin, and FACIT collagens (Fibril-Associated Collagens with Interrupted Triple helices), further demonstrates our cursory knowledge of the ECM in coordinated wound healing. Critical Issues: The manipulation and augmentation of ECM components in the healing wound is emerging in patient care, as demonstrated by the use of acellular dermal matrices, tissue scaffolds, and wound dressings or topical products bearing ECM proteins such as collagen, hyaluronan (HA), or elastin. Once thought of as neutral structural proteins, these molecules are now known to directly influence many aspects of cellular wound healing. Future Directions: The role that ECM molecules, such as CCN2, osteopontin, and secreted protein, acidic and rich in cysteine, play in signaling homing of fibroblast progenitor cells to sites of injury invites future research as we continue investigating the heterotopic origin of certain populations of fibroblasts in a healing wound. Likewise, research into differently sized fragments of the same polymeric ECM molecule is warranted as we learn that fragments of molecules such as HA and tenascin-C can have opposing effects on dermal fibroblasts.

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Crossref · 10.1089/wound.2014.0561

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Research works printed but not linked: 7

  1. Baur PS, 1975, Surg Gynecol Obstet, 141, 22
  2. Donaghue VM, Adv Wound Care, 11, 114
  3. 10.1042/bj3380637 · DOI
  4. Varkey M, 2014, Tissue Eng Part A, 20, 716
  5. Wester J, 1978, Lab Invest, 39, 298
  6. Olczyk P, 2013, Evid Based Complement Alternat Med, 2013, 290675
  7. Yeo TK, 1991, Am J Pathol, 138, 1437

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Metadata

Authors
Tracy, L. E., Minasian, R. A., & Caterson, E. J.
Affiliations
Brigham and Women's Hospital (US)
Venue
Advances in Wound Care
Published
2016-03
Volume
5
Issue
3
Pages
119-136
ISSN
  • 2162-1918 (ISSN-L)
  • 2162-1934
OpenAlex
W2004098988
Cited by
1,008
References
194
Citations by year
2026: 82 · 2025: 130 · 2024: 132 · 2023: 126 · 2022: 130 · 2021: 124 · 2020: 104 · 2019: 65 · 2018: 59 · 2017: 42 · 2016: 13
FWCI
2.28
Type
journal article
Language
en
Open access
Locations
  • Advances in Wound Care (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Wound Healing and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Connective Tissue Growth Factor Research
  • Physical Sciences › Materials Science › Biomaterials › Electrospun Nanofibers in Biomedical Applications
Keywords
extracellular matrix, dermal fibroblasts, wound healing, collagen, fibrin, fibronectin, proteoglycans, glycosaminoglycans, matricellular proteins, dermatopontin, acellular dermal matrix, tissue engineering scaffolds, wound dressings, hyaluronic acid, elastin, osteopontin, connective tissue growth factor, SARC, tenascin-C, fibroblast migration, transgenic animal models

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