Increased expression of the Abcg2 transporter during erythroid maturation plays a role in decreasing cellular protoporphyrin IX levels
- 15 March 2005
- journal article
- Published by American Society of Hematology in Blood
- Vol. 105 (6) , 2571-2576
- https://doi.org/10.1182/blood-2004-04-1566
Abstract
ABCG2/BCRP is a member of the adenosine triphosphate–binding cassette (ABC) transporter family and is expressed in intestine, kidney, and liver, where it modulates the absorption and excretion of xenobiotic compounds. ABCG2 is also expressed in hematopoietic stem cells and erythroid cells; however, little is known regarding its role in hematopoiesis. Abcg2 null mice have increased levels of protoporphyrin IX (PPIX) in erythroid cells, yet the mechanism for this remains uncertain. We have found that Abcg2 mRNA expression was up-regulated in differentiating erythroid cells, coinciding with increased expression of other erythroid-specific genes. This expression pattern was associated with significant amounts of ABCG2 protein on the membrane of mature peripheral blood erythrocytes. Erythroid cells engineered to express ABCG2 had significantly lower intracellular levels of PPIX, suggesting the modulation of PPIX level by ABCG2. This modulating activity was abrogated by treatment with a specific ABCG2 inhibitor, Ko143, implying that PPIX may be a direct substrate for the transporter. Taken together, our results demonstrate that ABCG2 plays a role in regulating PPIX levels during erythroid differentiation and suggest a potential role for ABCG2 as a genetic determinant in erythropoietic protoporphyria.Keywords
This publication has 30 references indexed in Scilit:
- Photodynamic therapy for cancerNature Reviews Cancer, 2003
- Low levels of ABCG2 expression in adult AML blast samplesBlood, 2002
- An exon 10 deletion in the mouse ferrochelatase gene has a dominant-negative effect and causes mild protoporphyriaBlood, 2002
- The Human ATP-Binding Cassette (ABC) Transporter SuperfamilyGenome Research, 2001
- Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase geneBiochemical and Biophysical Research Communications, 1991
- Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease.Journal of Clinical Investigation, 1991
- Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues.Proceedings of the National Academy of Sciences, 1987
- Splenic erythroblasts in anemia‐inducing friend disease: A source of cells for studies of erythropoietin‐mediated differentiationJournal of Cellular Physiology, 1984
- Genetic aspects of erythropoietic protoporphyriaAnnals of Human Genetics, 1984
- Erythropoietic protoporphyria 10 years experienceThe American Journal of Medicine, 1976