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From the Section of Orthodontics,*
UCLA School of
Dentistry, Los Angeles, California; the Departments of Restorative
Dentistry
and
Orthodontics,
Harvard School of Dental
Medicine, Boston, Massachusetts; the Department of Cell
Biology,§
Harvard Medical School, Boston,
Massachusetts; and the Jane and Jerry Weintraub Center for
Reconstructive Biotechnology,¶
Division of
Advanced Prosthodontics, Biomaterials and Hospital Dentistry, UCLA
School of Dentistry, Los Angeles, California
Bone wound created in intramembranous alveolar bone heals without
the formation of cartilage precursor tissue. However, the
expression of cartilage collagen mRNAs has been suggested. In this
report, we examined the expression and the potential role of
type IX collagen in bone restoration and remodeling. The sequence
specific polymerase chain reaction demonstrated the exclusive
expression of short transcriptional isoform of
1(IX) collagen
(Col9a1) in alveolar bone wound healing, while the long isoform
of Col9a1 transcript was absent. Type IX collagen was immunolocalized
in the preliminary matrix organized in granulation tissue before
trabecular bone formation in tooth extraction socket. In Col9a1-null
mutant mice, there were considerable variations in alveolar
bone wound healing with the absence of or abnormally organized
trabecular bone. Occasionally, unusual apposition of
cortical-bone-like layers in bone marrow space was observed. The
Col9a1-null mice indicated no growth retardation, and their
facial and long bones maintained the normal size and shape.
However, the primary spongiosa region of adult Col9a1 mutant
mice showed an abnormal trabecular bone structure associated with
abnormal immunostaining with the hypertrophic cartilage specific type X
collagen antibody. These data suggest that type IX collagen short
transcriptional variant is involved in the restoration and remodeling
processes of trabecular bone.
This article has been cited by other articles:
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P. J. McClive and A. H. Sinclair Type II and Type IX Collagen Transcript Isoforms Are Expressed During Mouse Testis Development Biol Reprod, May 1, 2003; 68(5): 1742 - 1747. [Abstract] [Full Text] [PDF] |
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