University of Oulu

Ritva Heljasvaara, Mari Aikio, Heli Ruotsalainen, Taina Pihlajaniemi, Collagen XVIII in tissue homeostasis and dysregulation — Lessons learned from model organisms and human patients, Matrix Biology, Volumes 57–58, 2017, Pages 55-75, ISSN 0945-053X,

Collagen XVIII in tissue homeostasis and dysregulation : lessons learned from model organisms and human patients

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Author: Heljasvaara, Ritva1,2; Aikio, Mari3,4; Ruotsalainen, Heli1;
Organizations: 1Oulu Center for Cell-Matrix Research, Biocenter Oulu, Faculty of Biochemistry and Molecular Medicine, University of Oulu, FIN-90014 Oulu, Finland
2Centre for Cancer Biomarkers CCBIO, Department of Biomedicine, University of Bergen, N-5009 Bergen, Norway
3Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA
4Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA
Format: article
Version: accepted version
Access: open
Online Access: PDF Full Text (PDF, 2.1 MB)
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Language: English
Published: Elsevier, 2017
Publish Date: 2017-10-13


Collagen XVIII is a ubiquitous basement membrane (BM) proteoglycan produced in three tissue-specific isoforms that differ in their N-terminal non-collagenous sequences, but share collagenous and C-terminal non-collagenous domains. The collagenous domain provides flexibility to the large collagen XVIII molecules on account of multiple interruptions in collagenous sequences. Each isoform has a complex multi-domain structure that endows it with an ability to perform various biological functions. The long isoform contains a frizzled-like (Fz) domain with Wnt-inhibiting activity and a unique domain of unknown function (DUF959), which is also present in the medium isoform. All three isoforms share an N-terminal laminin-G-like/thrombospondin-1 sequence whose specific functions still remain unconfirmed. The proteoglycan nature of the isoforms further increases the functional diversity of collagen XVIII. An anti-angiogenic domain termed endostatin resides in the C-terminus of collagen XVIII and is proteolytically cleaved from the parental molecule during the BM breakdown for example in the process of tumour progression. Recombinant endostatin can efficiently reduce tumour angiogenesis and growth in experimental models by inhibiting endothelial cell migration and proliferation or by inducing their death, but its efficacy against human cancers is still a subject of debate. Mutations in the COL18A1 gene result in Knobloch syndrome, a genetic disorder characterised mainly by severe eye defects and encephalocele and, occasionally, other symptoms. Studies with gene-modified mice have elucidated some aspects of this rare disease, highlighting in particular the importance of collagen XVIII in the development of the eye. Research with model organisms have also helped in determining other structural and biological functions of collagen XVIII, such as its requirement in the maintenance of BM integrity and its emerging roles in regulating cell survival, stem or progenitor cell maintenance and differentiation and inflammation. In this review, we summarise current knowledge on the properties and endogenous functions of collagen XVIII in normal situations and tissue dysregulation. When data is available, we discuss the functions of the distinct isoforms and their specific domains.

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Series: Matrix biology
ISSN: 0945-053X
ISSN-E: 1569-1802
ISSN-L: 0945-053X
Volume: 57-58
Pages: 55 - 75
DOI: 10.1016/j.matbio.2016.10.002
Type of Publication: A2 Review article in a scientific journal
Field of Science: 3111 Biomedicine
Funding: This study was supported by the Health Science Council of the Academy of Finland (Centre of Excellence 2012–2017 Grant 251314), by Sigrid Jusélius Foundation and by the Cancer Society of Northern Finland.
Academy of Finland Grant Number: 251314
Detailed Information: 251314 (Academy of Finland Funding decision)
Copyright information: © 2016. This manuscript version is made available under the CC-BY-NC-ND 4.0 license