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Prolactin/growth hormone–derived antiangiogenic peptides highlight a potential role of tilted peptides in angiogenesis
- Source :
- Proceedings of the National Academy of Sciences. 103:14319-14324
- Publication Year :
- 2006
- Publisher :
- Proceedings of the National Academy of Sciences, 2006.
-
Abstract
- Angiogenesis is a crucial step in many pathologies, including tumor growth and metastasis. Here, we show that tilted peptides exert antiangiogenic activity. Tilted (or oblique-oriented) peptides are short peptides known to destabilize membranes and lipid cores and characterized by an asymmetric distribution of hydrophobic residues along the axis when helical. We have previously shown that 16-kDa fragments of the human prolactin/growth hormone (PRL/GH) family members are potent angiogenesis inhibitors. Here, we demonstrate that all these fragments possess a 14-aa sequence having the characteristics of a tilted peptide. The tilted peptides of human prolactin and human growth hormone induce endothelial cell apoptosis, inhibit endothelial cell proliferation, and inhibit capillary formation both in vitro and in vivo . These antiangiogenic effects are abolished when the peptides' hydrophobicity gradient is altered by mutation. We further demonstrate that the well known tilted peptides of simian immunodeficiency virus gp32 and Alzheimer's β-amyloid peptide are also angiogenesis inhibitors. Taken together, these results point to a potential new role for tilted peptides in regulating angiogenesis.
- Subjects :
- Angiogenesis
Molecular Sequence Data
Retroviridae Proteins, Oncogenic
Neovascularization, Physiologic
Angiogenesis Inhibitors
Apoptosis
Peptide
Chick Embryo
Biology
Membrane Fusion
Alzheimer Disease
In vivo
Animals
Humans
Amino Acid Sequence
Peptide sequence
Cell Proliferation
chemistry.chemical_classification
Amyloid beta-Peptides
Multidisciplinary
Cell growth
Endothelial Cells
Gene Products, env
Biological Sciences
Peptide Fragments
Recombinant Proteins
In vitro
Prolactin
Rats
Molecular Weight
Endothelial stem cell
chemistry
Biochemistry
Growth Hormone
Liposomes
Cattle
Mutant Proteins
Hydrophobic and Hydrophilic Interactions
Viral Fusion Proteins
Subjects
Details
- ISSN :
- 10916490 and 00278424
- Volume :
- 103
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences
- Accession number :
- edsair.doi.dedup.....1471ff3d824ae56b9d0e8da26a6b1398