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Potential immunoregulatory role of heme oxygenase-1 in human milk: a combined biochemical and molecular modeling approach

Giovanni Li VoltiaCorresponding Author Information1email address, Fabio Galvanoa1, Alessandro Frigiolab, Salvatore Guccionec, Claudia Di Giacomoa, Stefano Fortec, Giovanni Tringalid, Massimo Carusode, Olayiwola Adedotun Adekoyaf, Diego Gazzologh

Received 4 March 2009; received in revised form 15 June 2009; accepted 22 June 2009. published online 02 November 2009.
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Abstract 

Human milk contains biological factors that are involved in a newborn's growth and immune system regulation. By integrating standard biochemical experimental protocols with computational methods, the present study investigates the presence of heme oxygenase-1 (HO-1), a cytoprotective enzyme, in human milk at different levels of maturation and in milk formulae. Furthermore, we evaluated cytokine and glutathione S-transferase (GSH) levels. Samples were collected from colostrum (on Day 1 after birth), from transition milk (on Postdelivery Days 7 and 14) and from mature milk (on Day 30 after delivery) in 14 healthy women. HO-1 protein, GSH and cytokines levels were measured using enzyme-linked immunosorbent assay and flow cytometry. HO-1 protein levels were significantly higher in colostrum (1.33 ng/ml; 5th centile 0.92; 95th centile 2.38) and in transition milk at 14 days (0.97 ng/ml; 5th centile 0.87; 95th centile 1.45) than in mature milk (0.9 ng/ml; 5th centile 0.8; 95th centile 1.38). Levels of HO-1 in milk formulae were similar to those in colostrum. No significant differences in GSH content were observed in mature milk, transition milk and colostrum, whereas significantly higher GSH levels were observed in milk formulae. No significant levels of cytokines, with the exception of interleukin-8, were found. Computational studies on the possible interactions between HO-1 and CD91 were carried out by a battery of softwares, namely, GRAMM (version 1.03), DALI, CLUSTALW (version 2.0), PatchDock and FireDock, mutually counterchecking and validating each other. The computational results, the strong convergence (to the same “solution”) of which finally leads to an “experimental-like” character, showed that HO-1 may bind to CD91, thus suggesting its major role as a new chaperokine in immune response regulation. These findings, which connect and integrate biochemical data and computational data interpretation, represent a synergistic and powerful means of conducting biological research.

a Department of Biological Chemistry, Medical Chemistry and Molecular Biology, University of Catania, 95125 Catania, Italy

b Perinatal Research Laboratory, IRCSS San Donato Milanese, 20097 Milan, Italy

c Department of Pharmaceutical Sciences, University of Catania, 95125 Catania, Italy

d Istituto di Ricerca Medica ed Ambientale, 95024 Acireale, Italy

e Istituto Oncologico del Mediterraneo, 95125 Catania, Italy

f Department of Pharmacology, Institute of Medical Biology, University of Tromsø, 9037 Tromsø, Norway

g Neonatal Intensive Care Unit, “Cesare Arrigo” Children Hospital, 15100 Alessandria, Italy

h Department of Pediatrics, G. Gaslini Children's University Hospital, 16167 Genoa, Italy

Corresponding Author InformationCorresponding author. Tel.: +39 95 7384081; fax: +39 95 7384220.

1 G. Li Volti and F. Galvano contributed equally to this work.

PII: S0955-2863(09)00140-5

doi:10.1016/j.jnutbio.2009.06.011

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