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Determination of hyaluronan molecular mass distribution in human breast milk.
Yuan, Han; Amin, Ripal; Ye, Xin; de la Motte, Carol A; Cowman, Mary K.
Afiliación
  • Yuan H; Department of Chemical and Biomolecular Engineering, Polytechnic School of Engineering, New York University, Brooklyn, NY 11201, USA.
  • Amin R; Department of Chemical and Biomolecular Engineering, Polytechnic School of Engineering, New York University, Brooklyn, NY 11201, USA; Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA; Department of Colorectal Surgery, Lerner Research Institute, Clevel
  • Ye X; Department of Chemical and Biomolecular Engineering, Polytechnic School of Engineering, New York University, Brooklyn, NY 11201, USA.
  • de la Motte CA; Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA; Department of Colorectal Surgery, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
  • Cowman MK; Department of Chemical and Biomolecular Engineering, Polytechnic School of Engineering, New York University, Brooklyn, NY 11201, USA. Electronic address: mary.cowman@nyu.edu.
Anal Biochem ; 474: 78-88, 2015 Apr 01.
Article en En | MEDLINE | ID: mdl-25579786
Hyaluronan (HA) in human milk mediates host responses to microbial infection via TLR4- and CD44-dependent signaling. Signaling by HA is generally size specific. Because pure HA with average molecular mass (M) of 35 kDa can elicit a protective response in intestinal epithelial cells, it has been proposed that human milk HA may have a bioactive low-M component. Here we report the size distribution of HA in human milk samples from 20 unique donors. A new method for HA analysis, employing ion exchange (IEX) chromatography to fractionate HA by size and specific quantification of each size fraction by competitive enzyme-linked sorbent assay (ELSA), was developed. When separated into four fractions, milk HA with M⩽20 kDa, M∼20 to 60 kDa, and M∼60 to 110 kDa comprised averages of 1.5, 1.4, and 2.0% of the total HA, respectively. The remaining 95% was HA with M⩾110 kDa. Electrophoretic analysis of the higher M HA from 13 samples showed nearly identical M distributions, with an average M of approximately 440 kDa. This higher M HA component in human milk is proposed to bind to CD44 and to enhance human beta defensin 2 (HBD2) induction by the low-M HA components.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ácido Hialurónico / Leche Humana Límite: Female / Humans Idioma: En Revista: Anal Biochem Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ácido Hialurónico / Leche Humana Límite: Female / Humans Idioma: En Revista: Anal Biochem Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos