Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP-3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10

S. S. Apte, K. Hayashi, Michael F Seldin, M. G. Mattei, M. Hayashi, B. R. Olsen

Research output: Contribution to journalArticle

122 Citations (Scopus)

Abstract

Remodeling of the extracellular matrix (ECM) is an essential component of normal development and is also involved in the pathogenesis of arthritis and the spread of cancer. The matrix metalloproteinases and their natural inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), play an important role in this context. We have isolated mouse cDNA clones encoding a novel member of the TIMP family, designated TIMP-3. We have assigned the Timp-3 locus to the [C1-D1] region of mouse chromosome 10 using both genetic and cytogenetic methods. The conceptual translation product of the Timp-3 cDNA shows a high degree of similarity with ChIMP-3, a recently cloned chicken metalloproteinase inhibitor, as well as significant structural similarity with the amino acid sequences of the previously isolated members of this family, TIMP-1 and TIMP-2. The pattern of expression of Timp-3 in the developing mouse embryo is distinct from that previously reported for Timp- 1. Timp-3 is expressed in cartilage and skeletal muscle, in myocardium, in the skin, oral and nasal epithelium, in the newborn mouse liver, in the epithelium of some tubular structures such as the developing bronchial tree, oesophagus, colon, urogenital sinus, bile duct, in the kidney, salivary glands, and in the choroid plexus of the brain. The patterns of Timp-3 expression in surface epithelia and in the epithelial lining of many tubular organs suggests that TIMP-3 may be involved in regulating ECM remodeling during the folding of epithelia and during the formation, branching, and expansion of epithelial tubes. In the mouse placenta, expression is seen in the trophoblast, raising the possibility that TIMP-3 may be involved in regulating trophoblastic invasion of the uterus. We propose a role for TIMP- 3 in musculoskeletal and cardiac development, in the morphogenesis of certain epithelial structures, and placental implantation.

Original languageEnglish (US)
Pages (from-to)177-197
Number of pages21
JournalDevelopmental Dynamics
Volume200
Issue number3
StatePublished - 1994
Externally publishedYes

Fingerprint

Tissue Inhibitor of Metalloproteinase-3
Tissue Inhibitor of Metalloproteinases
Chromosomes, Human, Pair 10
Cartilage
Epithelium
Muscles
Genes
Extracellular Matrix
Musculoskeletal Development
Complementary DNA
Tissue Inhibitor of Metalloproteinase-2
Tissue Inhibitor of Metalloproteinase-1
Choroid Plexus
Nasal Mucosa
Trophoblasts
Metalloproteases
Bile Ducts
Salivary Glands
Matrix Metalloproteinases
Morphogenesis

Keywords

  • Cartilage
  • Epithelium
  • Extracellular matrix
  • Metalloproteinases
  • Muscle
  • TIMP-3

ASJC Scopus subject areas

  • Cell Biology
  • Developmental Biology

Cite this

Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP-3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10. / Apte, S. S.; Hayashi, K.; Seldin, Michael F; Mattei, M. G.; Hayashi, M.; Olsen, B. R.

In: Developmental Dynamics, Vol. 200, No. 3, 1994, p. 177-197.

Research output: Contribution to journalArticle

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abstract = "Remodeling of the extracellular matrix (ECM) is an essential component of normal development and is also involved in the pathogenesis of arthritis and the spread of cancer. The matrix metalloproteinases and their natural inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), play an important role in this context. We have isolated mouse cDNA clones encoding a novel member of the TIMP family, designated TIMP-3. We have assigned the Timp-3 locus to the [C1-D1] region of mouse chromosome 10 using both genetic and cytogenetic methods. The conceptual translation product of the Timp-3 cDNA shows a high degree of similarity with ChIMP-3, a recently cloned chicken metalloproteinase inhibitor, as well as significant structural similarity with the amino acid sequences of the previously isolated members of this family, TIMP-1 and TIMP-2. The pattern of expression of Timp-3 in the developing mouse embryo is distinct from that previously reported for Timp- 1. Timp-3 is expressed in cartilage and skeletal muscle, in myocardium, in the skin, oral and nasal epithelium, in the newborn mouse liver, in the epithelium of some tubular structures such as the developing bronchial tree, oesophagus, colon, urogenital sinus, bile duct, in the kidney, salivary glands, and in the choroid plexus of the brain. The patterns of Timp-3 expression in surface epithelia and in the epithelial lining of many tubular organs suggests that TIMP-3 may be involved in regulating ECM remodeling during the folding of epithelia and during the formation, branching, and expansion of epithelial tubes. In the mouse placenta, expression is seen in the trophoblast, raising the possibility that TIMP-3 may be involved in regulating trophoblastic invasion of the uterus. We propose a role for TIMP- 3 in musculoskeletal and cardiac development, in the morphogenesis of certain epithelial structures, and placental implantation.",
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AU - Mattei, M. G.

AU - Hayashi, M.

AU - Olsen, B. R.

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