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Expression analysis of the novel gene collagen triple helix repeat containing-1 (Cthrc1)
Tahir Durmus1, Renée J LeClair, Kyoung-Sook Park
1Center for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, ME 04074, USA.
Insights
Collagen triple helix repeat containing-1 (Cthrc1) inhibits collagen synthesis and is found in developing and adult tissues. Its expression patterns suggest roles in skeletal development and epithelial-mesenchymal interactions.
Area of Science:
- Molecular Biology
- Developmental Biology
- Biochemistry
Background:
- Collagen triple helix repeat containing-1 (Cthrc1) is a novel secreted protein.
- Cthrc1 inhibits collagen matrix synthesis and is induced after arterial injury.
Purpose of the Study:
- To characterize the expression patterns of Cthrc1 in embryonic and postnatal murine tissues.
- To understand the potential functions of Cthrc1 based on its expression domains.
Main Methods:
- In situ hybridization
- Immunohistochemistry
Main Results:
- Cthrc1 expression was observed in various embryonic structures including the developing skeleton, neural tube, and kidney.
- In adult tissues, Cthrc1 was found in bone matrix, periosteum, kidney tubules, and epithelial-mesenchymal interfaces.
- Cthrc1 expression sites overlap with those of TGF-beta family members and interstitial collagens.
Conclusions:
- Cthrc1 plays a role in skeletal development and is present at key epithelial-mesenchymal interfaces.
- The expression profile of Cthrc1 suggests involvement in matrix regulation and tissue development.
Abstract:
We recently identified collagen triple helix repeat containing-1 (Cthrc1) as a novel gene induced in adventitial fibroblasts after arterial injury. Cthrc1 is a 30 kDa secreted protein that has the ability to inhibit collagen matrix synthesis. Cthrc1 is also glycosylated and retains a signal sequence consistent with the presence of Cthrc1 in the extracellular space. In injured arteries and skin wounds, we have found Cthrc1 expression to be associated with myofibroblasts and sites of collagen matrix deposition. Furthermore, we demonstrated that Cthrc1 inhibits collagen matrix deposition in vitro. Using in situ hybridization and immunohistochemistry, we characterized the expression domains of Cthrc1 during murine embryonic development and in postnatal tissues. In mouse embryos, Cthrc1 was expressed in the visceral endoderm, notochord, neural tube, developing kidney, and heart. Abundant expression of Cthrc1 was observed in the developing skeleton, i.e., in cartilage primordia, in growth plate cartilage with exclusion of the hypertrophic zone, in the bone matrix and periostium. Bones from adults showed expression of Cthrc1 only in the bone matrix and periostium while the articular cartilage lacked expression. Cthrc1 is typically expressed at epithelial-mesenchymal interfaces that include the epidermis and dermis, basal corneal epithelium, airway epithelium, esophagus epithelium, choroid plexus epithelium, and meninges. In the adult kidney, collecting ducts and distal tubuli expressed Cthrc1. Collectively, the sites of Cthrc1 expression overlap considerably with those reported for TGF-beta family members and interstitial collagens. The present study provides useful information towards the understanding of potential Cthrc1 functions.
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