Fibromodulin-deficient Mice Display Impaired Collagen Fibrillogenesis in Predentin as well as Altered Dentin Mineralization and Enamel Formation.
(2006) In Journal of Histochemistry and Cytochemistry 54(5). p.525-537- Abstract
- To determine the functions of fibromodulin (Fmod), a small leucine-rich keratan sulfate proteoglycan in tooth formation, we investigated the distribution of Fmod in dental tissues by immunohistochemistry and characterized the dental phenotype of 1-day-old Fmod-deficient mice using light and transmission electron microscopy. Immunohistochemistry was also used to compare the relative protein expression of dentin sialoprotein (DSP), dentin matrix protein-1 (DMP 1), bone sialoprotein (BSP), and osteopontin (OPN) between Fmod-deficient mice and wild-type mice. In normal mice and rats, Fmod immunostaining was mostly detected in the distal cell bodies of odontoblasts and in the stratum intermedium and was weaker in odontoblast processes and... (More)
- To determine the functions of fibromodulin (Fmod), a small leucine-rich keratan sulfate proteoglycan in tooth formation, we investigated the distribution of Fmod in dental tissues by immunohistochemistry and characterized the dental phenotype of 1-day-old Fmod-deficient mice using light and transmission electron microscopy. Immunohistochemistry was also used to compare the relative protein expression of dentin sialoprotein (DSP), dentin matrix protein-1 (DMP 1), bone sialoprotein (BSP), and osteopontin (OPN) between Fmod-deficient mice and wild-type mice. In normal mice and rats, Fmod immunostaining was mostly detected in the distal cell bodies of odontoblasts and in the stratum intermedium and was weaker in odontoblast processes and predentin. The absence of Fmod impaired dentin mineralization, increased the diameter of the collagen fibrils throughout the whole predentin, and delayed enamel formation. Immunohistochemistry provides evidence for compensatory mechanisms in Fmod-deficient mice. Staining for DSP and OPN was decreased in molars, whereas DMP 1 and BSP were enhanced. In the incisors, labeling for DSP, DMP 1, and BSP was strongly increased in the pulp and odontoblasts, whereas OPN staining was decreased. Positive staining was also seen for DMP 1 and BSP in secretory ameloblasts. Together these studies indicate that Fmod restricts collagen fibrillogenesis in predentin while promoting dentin mineralization and the early stages of enamel formation. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/148731
- author
- Goldberg, Michel ; Septier, Dominique ; Oldberg, Åke LU ; Young, Marian F and Ameye, Laurent G
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- tooth phenotype, osteopontin, dentin, enamel, dentin sialoprotein, bone sialoprotein, dentin matrix protein 1, fibromodulin
- in
- Journal of Histochemistry and Cytochemistry
- volume
- 54
- issue
- 5
- pages
- 525 - 537
- publisher
- Histochemical Society
- external identifiers
-
- pmid:16344330
- wos:000237101200004
- scopus:33646026687
- ISSN
- 0022-1554
- DOI
- 10.1369/jhc.5A6650.2005
- language
- English
- LU publication?
- yes
- id
- 3cda80aa-1e7e-4a61-93fc-bba67c1a9326 (old id 148731)
- alternative location
- http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16344330&dopt=Abstract
- date added to LUP
- 2016-04-01 17:01:48
- date last changed
- 2022-03-22 22:50:52
@article{3cda80aa-1e7e-4a61-93fc-bba67c1a9326, abstract = {{To determine the functions of fibromodulin (Fmod), a small leucine-rich keratan sulfate proteoglycan in tooth formation, we investigated the distribution of Fmod in dental tissues by immunohistochemistry and characterized the dental phenotype of 1-day-old Fmod-deficient mice using light and transmission electron microscopy. Immunohistochemistry was also used to compare the relative protein expression of dentin sialoprotein (DSP), dentin matrix protein-1 (DMP 1), bone sialoprotein (BSP), and osteopontin (OPN) between Fmod-deficient mice and wild-type mice. In normal mice and rats, Fmod immunostaining was mostly detected in the distal cell bodies of odontoblasts and in the stratum intermedium and was weaker in odontoblast processes and predentin. The absence of Fmod impaired dentin mineralization, increased the diameter of the collagen fibrils throughout the whole predentin, and delayed enamel formation. Immunohistochemistry provides evidence for compensatory mechanisms in Fmod-deficient mice. Staining for DSP and OPN was decreased in molars, whereas DMP 1 and BSP were enhanced. In the incisors, labeling for DSP, DMP 1, and BSP was strongly increased in the pulp and odontoblasts, whereas OPN staining was decreased. Positive staining was also seen for DMP 1 and BSP in secretory ameloblasts. Together these studies indicate that Fmod restricts collagen fibrillogenesis in predentin while promoting dentin mineralization and the early stages of enamel formation.}}, author = {{Goldberg, Michel and Septier, Dominique and Oldberg, Åke and Young, Marian F and Ameye, Laurent G}}, issn = {{0022-1554}}, keywords = {{tooth phenotype; osteopontin; dentin; enamel; dentin sialoprotein; bone sialoprotein; dentin matrix protein 1; fibromodulin}}, language = {{eng}}, number = {{5}}, pages = {{525--537}}, publisher = {{Histochemical Society}}, series = {{Journal of Histochemistry and Cytochemistry}}, title = {{Fibromodulin-deficient Mice Display Impaired Collagen Fibrillogenesis in Predentin as well as Altered Dentin Mineralization and Enamel Formation.}}, url = {{http://dx.doi.org/10.1369/jhc.5A6650.2005}}, doi = {{10.1369/jhc.5A6650.2005}}, volume = {{54}}, year = {{2006}}, }