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Adamts5, the gene encoding a proteoglycan-degrading metalloprotease, is expressed by specific cell lineages during mouse embryonic development and in adult tissues.

McCulloch, Daniel R., Le Goff, Carine, Bhatt, Sumantha, Dixon, Laura J., Sandy, John D. and Apte, Suneel S. 2009, Adamts5, the gene encoding a proteoglycan-degrading metalloprotease, is expressed by specific cell lineages during mouse embryonic development and in adult tissues., Gene expression patterns, vol. 9, no. 5, pp. 314-323, doi: 10.1016/j.gep.2009.02.006.

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Title Adamts5, the gene encoding a proteoglycan-degrading metalloprotease, is expressed by specific cell lineages during mouse embryonic development and in adult tissues.
Author(s) McCulloch, Daniel R.
Le Goff, Carine
Bhatt, Sumantha
Dixon, Laura J.
Sandy, John D.
Apte, Suneel S.
Journal name Gene expression patterns
Volume number 9
Issue number 5
Start page 314
End page 323
Total pages 10
Publisher Elsevier
Place of publication Amsterdam, The Netherlands
Publication date 2009-02-27
ISSN 1567-133X
1872-7298
Keyword(s) ADAMTS5
Adamts5
Aggrecanase
Development
Mouse
Transgenic
Arthritis
Osteoarthritis
Aggrecan
Versican
LacZ
b-Galactosidase
In situ hybridization
Peripheral nerve
Schwann cell
Smooth muscle
Skeletal muscle
Sympathetic ganglia
Inter-digital mesenchyme
Dorsal root ganglia
Choroid plexus
Cartilage
Tendon
Fibroblast
Summary The secreted metalloprotease ADAMTS5 is implicated in destruction of the cartilage proteoglycan aggrecan in arthritis, but its physiological functions are unknown. Its expression profile during embryogenesis and in adult tissues is therefore of considerable interest. β-Galactosidase (β-gal) histochemistry, enabled by a LacZ cassette inserted in the Adamts5 locus, and validated by in situ hybridization with an Adamts5 cRNA probe and ADAMTS5 immunohistochemistry, was used to profile Adamts5 expression during mouse embryogenesis and in adult mouse tissues. Embryonic expression was scarce prior to 11.5 days of gestation (E11.5) and noted only in the floor plate of the developing brain at E9.5. After E11.5 there was continued expression in brain, especially in the choroid plexus, peripheral nerves, dorsal root ganglia, cranial nerve ganglia, spinal and cranial nerves, and neural plexuses of the gut. In addition to nerves, developing limbs have Adamts5 expression in skeletal muscle (from E13.5), tendons (from E16.5), and inter-digital mesenchyme of the developing autopod (E13.5–15.5). In adult tissues, there is constitutive Adamts5 expression in arterial smooth muscle cells, mesothelium lining the peritoneal, pericardial and pleural cavities, smooth muscle cells in bronchi and pancreatic ducts, glomerular mesangial cells in the kidney, dorsal root ganglia, and in Schwann cells of the peripheral and autonomic nervous system. Expression of Adamts5 during neuromuscular development and in smooth muscle cells coincides with the broadly distributed proteoglycan versican, an ADAMTS5 substrate. These observations suggest the major contexts in which developmental and physiological roles could be sought for this protease.
Language eng
DOI 10.1016/j.gep.2009.02.006
Field of Research 060809 Vertebrate Biology
Socio Economic Objective 920199 Clinical Health (Organs, Diseases and Abnormal Conditions) not elsewhere classified
HERDC Research category C1.1 Refereed article in a scholarly journal
HERDC collection year 2009
Copyright notice ©2009, Elsevier B.V.
Persistent URL http://hdl.handle.net/10536/DRO/DU:30018573

Document type: Journal Article
Collections: Faculty of Health
School of Medicine
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Citation counts: TR Web of Science Citation Count  Cited 71 times in TR Web of Science
Scopus Citation Count Cited 73 times in Scopus Google Scholar Search Google Scholar
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Created: Tue, 08 Sep 2009, 16:47:45 EST by Daniel McCulloch

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