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Investigating serum factors promoting erythrocytic growth of Plasmodium falciparum
Authors:Asahi Hiroko  Kanazawa Tamotsu  Hirayama Nakami  Kajihara Yousei
Affiliation:Department of Parasitology, National Institute of Infectious Diseases, 23-1 Toyama 1-chome, Shinjuku-ku, Tokyo 162-8640, Japan. asahih@nih.go.jp
Abstract:The elucidation of factors inducing the growth of Plasmodium falciparum can provide critical information about the developmental mechanisms of this parasite and open the way to search for novel targets for malaria chemotherapy. The ability of components of a growth-promoting factor derived from bovine serum and various related substances to sustain growth of P. falciparum was characterized. A simple total lipid fraction (GFS-C) containing non-esterified fatty acids (NEFAs) as essential factors was noted to promote the parasite's growth. Various proteins from a variety of animals were tested, indicating the importance not only of GFS-C, but also of specific proteins, such as bovine and human albumin, in the parasite growth. Several combinations of the NEFAs tested sustained low parasite growth. Among various phospholipids and lysophospholipids tested, lysophosphatidylcholine containing C-18 unsaturated fatty acids was found to sustain the complete development of the parasite in the presence of bovine albumin. Several other lysophospholipids can partially support growth of P. falciparum.
Keywords:ALB, albumin   ANOVA, multifactorial analysis of variance   BSAF, NEFA-free ALB from bovine   C16:0, hexadecanoic acid   C16:1, cis-9-hexadecenoic acid   C18:0, octadecanoic acid   C18:1, cis-9-octadecenoic acid   C18:2, cis,cis-9,12-octadecadienoic acid   C18:3, cis,cis,cis-6,9,12-octadecatrienoic acid   C20:4, cis-5,8,11,14-eicosatetraenoic acid   C20:5, cis-5,8,11,14,17-eicosapentaenoic acid   C22:6, cis-4,7,10,13,16,19-docosahexaenoic acid   CDKs, cyclin-dependent protein kinases   CDPKs, calcium-dependent protein kinases   CHOL, cholesterol   CRPMI, basal medium   DGs, diglycerides   FBS, fetal bovine serum   GFS, a growth-promoting fraction derived from adult bovine serum   GFS-C, a total simple lipid fraction obtained from GFS   GFSRPMI, CRPMI containing 10% GFS   GFS-WM, a total complex lipid fraction obtained from GFS   Hepes, 4-(2-hydroxyethyl)-piperazine ethanesulfonic acid   HS, human serum   HSRPMI, CRPMI containing 10% HS   LPA, lysophosphatidic acid   18:1 LPA, cis-9-oleoyl LPA   LPC, lysophosphatidylcholine   12:0 LPC, lauroyl LPC   14:0 LPC, myristoyl LPC   16:0 LPC, palmitoyl LPC   18:0 LPC, stearoyl LPC   18:1 LPC, cis-9-oleoyl LPC   18:2 LPC, cis-9-linoleoyl LPC   18:U LPC, LPC containing primarily C-18 unsaturated fatty acids   LPC-brain, LPC from bovine brain   LPCRPMI, CRPMI containing 3 mg/ml BSAF and 40 μg/ml 18:U LPC   LPE, lysophosphatidyl ethanolamine   LPI, lysophosphatidyl inositol   LPS, lysophosphatidyl serine   Lyso PAF, γ-O-alkyl LPC   MAPK, mitogen-activated protein kinase   MEK, MAPK/extracellular signal-regulated kinase kinase   MGs, monoglycerides   NEFA, non-esterified fatty acid   OD650, absorbance at 650 nm   8:0 PA, dioctanoyl phosphatidic acid   18:1 PA, cis-9-dioleoyl phosphatidic acid   PAF, β-acetyl-γ-O-alkyl PC   PC, phosphatidylcholine   PE, phosphatidyl ethanolamine   PI, phosphatidyl inositol   PI-bovine, PI from bovine liver   PI-soybean, PI from soybean   PKC, protein kinase C   PLs, phospholipids   pLDH, parasite lactate dehydrogenase   PS, phosphatidyl serine   PTK, protein tyrosine kinase   RBCs, red blood cells   SD, standard deviation   SM, sphingomyelin   S-1-P, sphingosine 1-phosphate   SPC, sphingosylphosphorylcholine   sphingosine,   smallcaps"  >d- sphingosine
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