Journal article
Dimeric but not monomeric α-lactalbumin potentiates apoptosis by up regulation of ATF3 and reduction of histone deacetylase activity in primary and immortalised cells
JA Sharp, AJ Brennan, G Polekhina, DB Ascher, C Lefevre, KR Nicholas
Cellular Signalling | ELSEVIER SCIENCE INC | Published : 2017
Abstract
α-lactalbumin is a protein of dual function found in milk of most mammals. α-lactalbumin binds β-1,4-galactosyltransferase to form the regulatory subunit for lactose synthesis and has also been shown to cause cell death. This study shows, for the first time, that α-lactalbumin isolated in a rare 28 kDa dimeric form induces cell death, while 14 kDa monomeric α-lactalbumin is inactive. In contrast to the casein derived and chemically induced α-lactalbumin variants, MAL and HAMLET/BAMLET, the effects of 28 kDa α-lactalbumin are calcium independent and, unlike MAL and HAMLET, 28 kDa α-lactalbumin dimer causes cell death of primary mammary cells and a variety of immortalised cell lines, which are..
View full abstractGrants
Funding Acknowledgements
We acknowledge support of Contract grant sponsor: Geoffrey Gardiner Foundation, CRC for Co-operative Research of Innovative Dairy Products and Dairy Australia and NHMRC through the Career Development Award to GP and the Victorian State Government Operational Infrastructure Support Program. DBA was an Australian Postgraduate Award Scholar and a recipient of a St. Vincent's Institute Foundation Scholarship sponsored by Colin North and Major Engineering.