Chloroquine-resistant isoforms of the Plasmodium falciparum chloroquine resistance transporter acidify lysosomal pH in HEK293 cells more than chloroquine-sensitive isoforms

David C. Reeves, David A. Liebelt, Viswanathan Lakshmanan, Paul D. Roepe, David A. Fidock, Myles Akabas

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

The emergence of chloroquine-resistant Plasmodium falciparum malaria imperils the lives of millions of people in Africa, Southeast Asia and South America. Chloroquine resistance is associated with mutations in the P. falciparum chloroquine resistance transporter (PfCRT). We expressed chloroquine-sensitive (HB3) and resistant (Dd2) pfcrt alleles in HEK293 human embryonic kidney cells. PfCRT localized to the lysosomal limiting membrane and was not detected in the plasma membrane. We observed significant acidification of lysosomes containing PfCRT HB3 and Dd2, with Dd2 acidifying significantly more than HB3. A mutant HB3 allele expressing the K76T mutation (earlier found to be key for chloroquine resistance) acidified to the same extent as Dd2, whereas the acidification by a Dd2 allele expressing the T76K "back mutation" was significantly less than Dd2. Thus, the amino acid at position 76 is both an important determinant of chloroquine resistance in parasites and of lysosomal acidification following heterologous expression. PfCRT may be capable of modulating the pH of the parasite digestive vacuole, and thus chloroquine availability. Chloroquine accumulation and glycyl-phenylalanine-2-naphthylamide-induced release of lysosomal Ca2+ stores were unaffected by PfCRT expression. Cytoplasmic domain mutations did not alter PfCRT sorting to the lysosomal membrane. This heterologous expression system will be useful to characterize PfCRT protein structure and function, and elucidate its molecular role in chloroquine resistance.

Original languageEnglish (US)
Pages (from-to)288-299
Number of pages12
JournalMolecular and Biochemical Parasitology
Volume150
Issue number2
DOIs
StatePublished - Dec 2006

Fingerprint

HEK293 Cells
Chloroquine
Protein Isoforms
Mutation
Alleles
Parasites
Southeastern Asia
Membranes
Plasmodium falciparum PfCRT protein
Falciparum Malaria
South America
Vacuoles
Lysosomes
Phenylalanine
Cell Membrane
Kidney
Amino Acids

Keywords

  • Acidification
  • Chloroquine resistance
  • Lysosome
  • Malaria
  • PfCRT

ASJC Scopus subject areas

  • Molecular Biology
  • Parasitology

Cite this

Chloroquine-resistant isoforms of the Plasmodium falciparum chloroquine resistance transporter acidify lysosomal pH in HEK293 cells more than chloroquine-sensitive isoforms. / Reeves, David C.; Liebelt, David A.; Lakshmanan, Viswanathan; Roepe, Paul D.; Fidock, David A.; Akabas, Myles.

In: Molecular and Biochemical Parasitology, Vol. 150, No. 2, 12.2006, p. 288-299.

Research output: Contribution to journalArticle

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