Identification of enzymes responsible for the metabolism of heme in human platelets

J Biol Chem. 1998 Dec 11;273(50):33342-6. doi: 10.1074/jbc.273.50.33342.

Abstract

The major enzymes involved in the degradation of heme were identified in human platelets. It was determined that heme oxygenase activity levels in umbilical cord blood platelets were higher, whereas biliverdin reductase activity levels were comparable with that found in platelets from adults. In membranes prepared from adenosine diphosphate-activated platelets, UDP-glucuronic acid-dependent bilirubin conjugation was detected, whereas activity was negligible in unactivated platelets and undetected in serum and heat-inactivated platelets, and in platelets prepared from umbilical cord blood. Platelet fractions were analyzed by Western blot and shown to express heme oxygenase, biliverdin reductase, and UDP-glucuronosyltransferases, and there was concordance with known developmental profiles found in other tissues. Heme oxygenase expression was higher, whereas UGT expression was lower, in neonatal compared with adult platelets. These data suggest that platelets are involved in multiple steps of heme and bilirubin metabolism and that developmental regulation of these enzymes may be similar to that in other human tissues.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Animals
  • Blood Platelets / enzymology*
  • Blood Platelets / metabolism
  • Gene Expression Regulation, Developmental
  • Gene Expression Regulation, Enzymologic
  • Glucuronosyltransferase / genetics
  • Glucuronosyltransferase / metabolism*
  • Heme / metabolism*
  • Heme Oxygenase (Decyclizing) / metabolism*
  • Humans
  • In Vitro Techniques
  • Infant, Newborn
  • Male
  • Oxidoreductases / metabolism*
  • Oxidoreductases Acting on CH-CH Group Donors*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Heme
  • Oxidoreductases
  • Heme Oxygenase (Decyclizing)
  • Oxidoreductases Acting on CH-CH Group Donors
  • biliverdin reductase
  • Glucuronosyltransferase