Literature DB >> 3541986

Morphological and histochemical events during first bone formation in embryonic chick limbs.

D G Pechak, M J Kujawa, A I Caplan.   

Abstract

Staged embryos from White Leghorn chicken eggs were used to assemble a detailed morphological, cellular and molecular picture of the complex events of first-bone formation. To provide these details, light and electron microscopic, histochemical and immunocytochemical techniques were used to establish a temporal sequence for long bone development in chick wing and leg from Hamburger-Hamilton stage 29 through stage 35. Three distinctive cell regions can be morphologically identified by stage 28 (leg) or 29 (wing) at the mid-diaphysis. These regions are: 1. an outer grouping of loose mesenchymal and myogenic cells, 2. an osteoprogenitor layer which will later divide to maintain this progenitor layer in a brickwork or stacked configuration and to produce round, tightly packed osteoblasts, and 3. a core (rod) of cartilage. First bone is laid down just outside the cartilage core, initially as a layer of Type I collagen-rich osteoid which later becomes mineralized. Vascular elements then come to reside above this mineral layer, and osteoid is laid down between vascular elements and eventually above them to form a second layer of trabecular bone. As this radial formation of layers of bone is progressing, so too is the proximal and distal expansion of the first bone forming process. A model is presented which considers that chondrogenic and osteogenic cell commitment occur simultaneously in early limb development and that it is the expression of the osteogenic phenotype which governs the boundaries of cartilage development. Importantly, the vasculature plays a key role in the patterning of bone formation well before it enters the cartilaginous core at stage 35 and participates in the erosion of the core. While this report is restricted to events occurring through stage 35, it relies on data presented in a companion report detailing later bone development and remodeling (Pechak et al; Bone 1986) and emphasizes that the cartilage model does not provide the scaffolding for bone but rather defines the marrow space.

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Year:  1986        PMID: 3541986     DOI: 10.1016/8756-3282(86)90004-9

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  21 in total

1.  Scleral fibroblasts of the chick embryo differentiate into chondrocytes in soft-agar culture.

Authors:  K Watanabe; K Yagi; Y Ohya; K Kimata
Journal:  In Vitro Cell Dev Biol       Date:  1992 Sep-Oct

2.  Immunohistochemical localization of a approximately 66 kD glycosylated phosphoprotein during development of the embryonic chick tibia.

Authors:  S P Bruder; A I Caplan; Y Gotoh; L C Gerstenfeld; M J Glimcher
Journal:  Calcif Tissue Int       Date:  1991-06       Impact factor: 4.333

Review 3.  New era of cell-based orthopedic therapies.

Authors:  Arnold I Caplan
Journal:  Tissue Eng Part B Rev       Date:  2009-06       Impact factor: 6.389

4.  The role of cartilage canals in endochondral and perichondral bone formation: are there similarities between these two processes?

Authors:  Michael J F Blumer; Stefano Longato; Elisabeth Richter; Maria Teresa Pérez; Kadriye Zeynep Konakci; Helga Fritsch
Journal:  J Anat       Date:  2005-04       Impact factor: 2.610

5.  An ultrastructural study of cartilage resorption at the site of initial endochondral bone formation in the fetal mouse mandibular condyle.

Authors:  S Shibata; S Suzuki; Y Yamashita
Journal:  J Anat       Date:  1997-07       Impact factor: 2.610

6.  Intramembranous osteogenesis and angiogenesis in the chick embryo.

Authors:  T J Thompson; P D Owens; D J Wilson
Journal:  J Anat       Date:  1989-10       Impact factor: 2.610

7.  Nitric oxide-mediated vasodilation increases blood flow during the early stages of stress fracture healing.

Authors:  Ryan E Tomlinson; Kooresh I Shoghi; Matthew J Silva
Journal:  J Appl Physiol (1985)       Date:  2013-12-19

8.  Clinical application of human mesenchymal stromal cells for bone tissue engineering.

Authors:  Anindita Chatterjea; Gert Meijer; Clemens van Blitterswijk; Jan de Boer
Journal:  Stem Cells Int       Date:  2010-11-11       Impact factor: 5.443

9.  Angiogenesis is required for stress fracture healing in rats.

Authors:  Ryan E Tomlinson; Jennifer A McKenzie; Anne H Schmieder; Gregory R Wohl; Gregory M Lanza; Matthew J Silva
Journal:  Bone       Date:  2012-10-05       Impact factor: 4.398

10.  Altered fracture repair in the absence of MMP9.

Authors:  Céline Colnot; Zachary Thompson; Theodore Miclau; Zena Werb; Jill A Helms
Journal:  Development       Date:  2003-09       Impact factor: 6.868

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