Haem Biosynthesis and Antioxidant Enzymes in Circulating Cells of Acute Intermittent Porphyria Patients

PLoS One. 2016 Oct 27;11(10):e0164857. doi: 10.1371/journal.pone.0164857. eCollection 2016.

Abstract

The aims of the present study were to explore the expression pattern of haem biosynthesis enzymes in circulating cells of patients affected by two types of porphyria (acute intermittent, AIP, and variegate porphyria, VP), together with the antioxidant enzyme pattern in AIP in order to identify a possible situation of oxidative stress. Sixteen and twelve patients affected by AIP and VP, respectively, were analysed with the same numbers of healthy matched controls. Erythrocytes, neutrophils and peripheral blood mononuclear cells (PBMCs) were purified from blood, and RNA and proteins were extracted for quantitative real time PCR (qRT-PCR) and Western-blot analysis, respectively. Porhobilinogen deaminase (PBGD) and protoporphyrinogen oxidase (PPOX) gene and protein expression was analysed. Antioxidant enzyme activity and gene expression were additionally determined in blood cells, together with protein carbonyl content in plasma. PBMCs isolated from AIP patients presented low mRNA levels of PBGD when compared to controls, while PBMCs isolated from VP patients presented a decrease in PPOX mRNA. PPOX protein content was higher in AIP patients and lower in VP patients, compared to healthy controls. Regarding antioxidant enzymes, PBMCs and erythrocyte superoxide dismutase (SOD) presented statistically significant higher activity in AIP patients compared to controls, while catalase activity tended to be lower in these patients. No differences were observed regarding antioxidant gene expression in white blood cells. Circulating cells in AIP and VP patients present altered expression of haem biosynthetic enzymes, which could be useful for the differential diagnosis of these two types of porphyria in certain difficult cases. AIP patients present a condition of potential oxidative stress similar to VP patients, evidenced by the post-transcriptional activation of SOD and possible catalase impairment.

MeSH terms

  • Blotting, Western
  • Case-Control Studies
  • Erythrocytes / enzymology
  • Female
  • Gene Expression
  • Heme / analysis
  • Heme / biosynthesis*
  • Humans
  • Hydroxymethylbilane Synthase / blood*
  • Leukocytes / enzymology
  • Male
  • Oxidative Stress
  • Porphyria, Acute Intermittent / blood
  • Porphyria, Acute Intermittent / enzymology
  • Porphyria, Variegate / blood
  • Porphyria, Variegate / enzymology
  • Protoporphyrinogen Oxidase / blood*
  • Real-Time Polymerase Chain Reaction

Substances

  • Heme
  • Protoporphyrinogen Oxidase
  • Hydroxymethylbilane Synthase

Grants and funding

This work has been granted by “Acción Estratégica en Salud del Ministro de Ciencia e Innovación” (DPS2008-07033-C03-03), Programme of Promotion of Biomedical Research and Health Sciences, Projects 11/01791, Red Predimed-RETIC RD06/0045/1004, CIBERobn CB12/03/30038, Balearic Island Government and FEDER funds (35/2011 and 23/2012), PROMETEO/2012/007 from Generalitat Valenciana to ER. ER is recipient of Instituto de Salud Carlos III-FEDER (PS09/01093) and Fundacion Salud 2000-Merck Serono grants. LC-Q was recipient of a CONACYT-Mexico (ref 197139) fellowship. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.