Milk osteopontin promotes intestinal development by up-regulating the expression of integrin αvβ3 and CD44

Osteopontin (OPN) is a pleiotropic protein involved in numerous biological processes such as cell proliferation and differentiation. Since OPN is abundantly present in milk and is known to be relatively resistant to in vitro gastrointestinal digestion, the current study aimed to investigate the roles of oral intake of milk OPN in intestinal development using an established OPN knockout (KO, OPN-/-) mouse model, in which wild-type (WT, OPN+/+) mouse pups were nursed by either WT (OPN+/+OPN+ group) or OPN KO dams (OPN+/+OPN- group; +/+ indicates genotype and - indicates milk without OPN), receiving milk with or without OPN from postnatal days 0 to 21 (P0-P21). Our results showed that milk OPN is resistant to in vivo digestion. Compared to OPN+/+OPN- pups, OPN+/+OPN+ pups at P4 and P6 had significantly longer small intestines, at P10 and P20 had larger inner jejunum surfaces, and at P30 exhibited more mature/differentiated intestines, as revealed by higher activities of alkaline phosphatase in brush border and more goblet cells, enteroendocrine cells, and Paneth cells. qRT-PCR and immunoblotting results showed that milk OPN increased the expression of integrin av, integrin beta 3, and CD44 in jejunum of mouse pups (P10, P20, and P30). Immunohistochemistry analysis showed that both integrin alpha v beta 3 and CD44 are localized in jejunum crypts. In addition, milk OPN increased the phosphorylation/activation of the ERK, PI3K/Akt, Wnt, and FAK signaling pathways. In summary, oral intake of milk OPN in early life promotes intestinal proliferation and differentiation by upregulating the expression of integrin alpha v beta 3 and CD44 and thus regulates OPN-integrin alpha v beta 3 and OPN-CD44 mediated cellular signaling pathways.

Automated summary

This study found that oral intake of milk containing OPN can promote intestinal development in early life by increasing cell proliferation and activating cellular signaling pathways.