Literature DB >> 10989939

Localization of alkaline phosphatase and osteopontin during matrix mineralization in the developing cartilage of coccygeal vertebrae.

T Sasaki1, N Amizuka, K Irie, S Ejiri, H Ozawa.   

Abstract

We observed the manner in which alkaline phosphatase (ALPase) and osteopontin were localized in the cartilage and intramembranous bone of coccygeal vertebrae during matrix mineralization, shedding considerable light on the manner in which they develop. In the cartilage matrix of coccygeal vertebrae, we observed the localization of ALPase activity in the boundary of the proliferative and the hypertrophic zones. Granular nodules of mineralization were consistently found in the boundary of both zones, and increased in size when close to the hypertrophic zone. While osteopontin was rarely present in the early stages of mineralization, its localization along the margins of mineralized matrices in the hypertrophic zone was prominent. In contrast to cartilage, mineralized nodules in the intramembranous bone in the mid-portion of the vertebra displayed osteopontin-immunoreactivity, indicating its early synthesis and subsequent accumulation to early-stage mineralized nodules. When blood vessels, accompanied by osteoblastic and osteoclastic cell populations, invaded the cartilage, osteopontin was localized in the lower region of the hypertrophic zone, despite its maintaining the localization of ALPase and early-stage mineralization. Thus, our investigation demonstrated ALPase activity consistent with early-stage mineralization in the cartilage matrix. However, the fact that osteopontin-localization could not be pinpointed might account for its multifunctionality as concerns both the regulation of mineralization and the attachment of migrating osteogenic and osteoclastic cells to the mineralized matrix.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10989939     DOI: 10.1679/aohc.63.271

Source DB:  PubMed          Journal:  Arch Histol Cytol        ISSN: 0914-9465


  5 in total

1.  A neocartilage ideal for extracellular matrix macromolecule immunolocalization.

Authors:  A B Parikh; G M Lee; I V Tchivilev; R D Graff
Journal:  Histochem Cell Biol       Date:  2003-10-31       Impact factor: 4.304

2.  Runx2/Cbfa1, but not loss of myocardin, is required for smooth muscle cell lineage reprogramming toward osteochondrogenesis.

Authors:  Mei Y Speer; Xianwu Li; Pranoti G Hiremath; Cecilia M Giachelli
Journal:  J Cell Biochem       Date:  2010-07-01       Impact factor: 4.429

3.  Detecting microcalcifications in atherosclerotic plaques by a simple trichromic staining method for epoxy embedded carotid endarterectomies.

Authors:  M Relucenti; R Heyn; L Petruzziello; G Pugliese; M Taurino; G Familiari
Journal:  Eur J Histochem       Date:  2010-07-14       Impact factor: 3.188

4.  Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis.

Authors:  Amitabha Bandyopadhyay; Kunikazu Tsuji; Karen Cox; Brian D Harfe; Vicki Rosen; Clifford J Tabin
Journal:  PLoS Genet       Date:  2006-11-06       Impact factor: 5.917

Review 5.  On the evolutionary relationship between chondrocytes and osteoblasts.

Authors:  Patsy Gómez-Picos; B Frank Eames
Journal:  Front Genet       Date:  2015-09-23       Impact factor: 4.599

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.