Hemoglobin-derived Peptides as Novel Type of Bioactive Signaling Molecules

Author(s)

Gomes, Ivone ^[1] ; Dale, Camila S. ^[2] ; Casten, Kimbie ^[1] ; Geigner, Miriam A. ^[3] ; Gozzo, Fabio C. ^[4] ; Ferro, Emer S. ^[5] ; Heimann, Andrea S. ^[3] ; Devi, Lakshmi A. ^[1]

Affiliation

^[1] Mt Sinai Sch Med, Dept Pharmacol & Syst Therapeut, New York, NY 10029 - USA

^[2] Sirio Libanes Hosp, Lab Neuromodulat & Expt Pain, Inst Teaching & Res, BR-01308000 Sao Paulo - Brazil

^[3] Proteimax Biotechnol Ltda, BR-06713330 Cotia, SP - Brazil

^[4] Univ Estadual Campinas, Inst Chem, BR-13083970 Campinas, SP - Brazil

^[5] Univ Sao Paulo, Dept Dev & Cell Biol, Inst Biomed Sci, BR-05508900 Sao Paulo - Brazil

• Document type: Review article
• Source: AAPS JOURNAL; v. 12, n. 4, p. 658-669, DEC 2010.
• Web of Science Citations: 56

Abstract

Most bioactive peptides are generated by proteolytic cleavage of large precursor proteins followed by storage in secretory vesicles from where they are released upon cell stimulation. Examples of such bioactive peptides include peptide neurotransmitters, classical neuropeptides, and peptide hormones. In the last decade, it has become apparent that the breakdown of cytosolic proteins can generate peptides that have biological activity. A case in point and the focus of this review are hemoglobin-derived peptides. In vertebrates, hemoglobin (Hb) consists of a tetramer of two alpha- and two beta-globin chains each containing a prosthetic heme group, and is primarily involved in oxygen delivery to tissues and in redox reactions (Schechter Blood 112:3927-3938, 2008). The presence of alpha- and/or beta-globin chain in tissues besides red blood cells including rodent and human brain and peripheral tissues (Liu et al. Proc Natl Acad Sci USA 96:6643-6647, 1999; Newton et al. J Biol Chem 281:5668-5676, 2006; Wride et al. Mol Vis 9:360-396, 2003; Setton-Avruj Exp Neurol 203:568-578, 2007; Ohyagi et al. Brain Res 635:323-327, 1994; Schelshorn et al. J Cereb Blood Flow Metab 29:585-595, 2009; Richter et al. J Comp Neurol 515:538-547, 2009) suggests that globins and/or derived peptidic fragments might play additional physiological functions in different tissues. In support of this hypothesis, a number of Hb-derived peptides have been identified and shown to have diverse functions (Ivanov et al. Biopoly 43:171-188, 1997; Karelin et al. Neurochem Res 24:1117-1124, 1999). Modern mass spectrometric analyses have helped in the identification of additional Hb peptides (Newton et al. J Biol Chem 281:5668-5676, 2006; Setton-Avruj Exp Neurol 203:568-578, 2007; Gomes et al. FASEB J 23:3020-3029, 2009); the molecular targets for these are only recently beginning to be revealed. Here, we review the status of the Hb peptide field and highlight recent reports on the identification of a molecular target for a novel set of Hb peptides, hemopressins, and the implication of these peptides to normal cell function and disease. The potential therapeutic applications for these Hb-derived hemopressin peptides will also be discussed. (AU)

• FAPESP's process: 04/14258-0 - Conformation-specific antibodies: proposal for generation of antibodies directed at receptors linked to active G protein (GPCRs)
• Grantee: Andrea Sterman Heimann
• Support Opportunities: Research Grants - Innovative Research in Small Business - PIPE
• FAPESP's process: 04/04933-2 - Molecular cell biology of oligopeptidases
• Grantee: Emer Suavinho Ferro
• Support Opportunities: Research Projects - Thematic Grants