Abstract |
Procollagen processing is essential for organ development and tissue functions. Both procollagen C- proteinase enhancer 1 (PCPE1) and secreted frizzled-related protein 2 (sFRP2) play vital roles in collagen formation via regulating the procollagen C- proteinase activity of bone morphogenetic protein 1 (BMP1). However, whether the two proteins exert a synergistic effect on BMP1 activity remains unclear. Here, simultaneous knockdown of sFRP2 and PCPE1 led to less collagen formation in mouse embryonic fibroblasts and dorsalized phenotypes in zebrafish embryos. Further studies revealed a direct interaction between the Frizzled domain of sFRP2 and the complement/Uegf/BMP-1 domain of PCPE1, which enhances the cleavage activity of BMP1 on procollagen. These results suggest that double silencing of sFRP2 and PCPE1 may provide a strategy for treating fibrosis diseases caused by collagen deposition.
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Authors | Qin Zhu, Wei Guo, Shengjie Zhang, Yang Feng, Xiao Wang, Libin Zhou, Guo-Ru Huang |
Journal | FEBS letters
(FEBS Lett)
Vol. 593
Issue 1
Pg. 119-127
(01 2019)
ISSN: 1873-3468 [Electronic] England |
PMID | 30411347
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2018 Federation of European Biochemical Societies. |
Chemical References |
- Extracellular Matrix Proteins
- Glycoproteins
- Membrane Proteins
- Pcolce protein, mouse
- Sfrp2 protein, mouse
- Sfrp2 protein, zebrafish
- Zebrafish Proteins
- Bone Morphogenetic Protein 1
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Topics |
- Animals
- Binding Sites
- Body Patterning
- Bone Morphogenetic Protein 1
(metabolism)
- Cells, Cultured
- Extracellular Matrix Proteins
(chemistry, genetics, metabolism)
- Fibroblasts
(cytology, metabolism)
- Gene Knockdown Techniques
- Glycoproteins
(chemistry, genetics, metabolism)
- Membrane Proteins
(genetics, metabolism)
- Mice
- Zebrafish
(embryology, growth & development, metabolism)
- Zebrafish Proteins
(chemistry, genetics, metabolism)
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