Biosensing of opioids using frog melanophores

被引:23
作者
Karlsson, AM
Bjuhr, K
Testorf, M
Öberg, PÅ
Lerner, E
Lundström, I
Svensson, SPS [1 ]
机构
[1] Fac Hlth Sci, Dept Med & Care, SE-58185 Linkoping, Sweden
[2] Linkoping Univ, Dept Biomed Engn, SE-58185 Linkoping, Sweden
[3] Bunsen Rush Labs, Dallas, TX USA
[4] Linkoping Univ, Dept Phys & Measurement Technol, SE-58183 Linkoping, Sweden
关键词
biosensor; opioids; chromatophores; melanophores; morphine; DAMGO;
D O I
10.1016/S0956-5663(01)00284-6
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Spectacular color changes of fishes, frogs and other lower vertebrates are due to the motile activities of specialized pigment containing cells. Pigment cells are interesting for biosensing purposes since they provide an easily monitored physiological phenomenon. Melanophores, containing dark brown melanin pigment granules, constitute an important class of chromatophores. Their melanin-filled pigment granules may be stimulated to undergo rapid dispersion throughout the melanophores (cells appear dark), or aggregation to the center of the melanophores (cells appear light). This simple physiological response can easily be measured in a photometer. Selected G protein coupled receptors can be functionally expressed in Cultured frog melanophores. Here, we demonstrate the use of recombinant frog melanophores as a biosensor for the detection of opioids. Melanophores were transfected with the human opioid receptor 3 and used for opiate detection. The response to the opioid receptor agonist morphine and a synthetic opioid peptide was analyzed by absorbance readings in an aggregation assay. It was shown that both agonists caused aggregation of pigment granules in the melanophores, and the cells appeared lighter. The pharmacology of the expressed receptors was very similar to its mammalian counterpart, as evidenced by competitive inhibition by increasing concentrations of the opioid receptor inhibitor naloxone. Transfection of melanophores with selected receptors enables the creation of numerous melanophore biosensors, which respond selectively to certain substances. The melanophore biosensor has potential use for measurement of substances in body fluids such as saliva, blood plasma and urine. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:331 / 335
页数:5
相关论文
共 20 条
  • [1] ACTION OF LIGHT ON FROG PIGMENT-CELLS IN CULTURE
    DANIOLOS, A
    LERNER, AB
    LERNER, MR
    [J]. PIGMENT CELL RESEARCH, 1990, 3 (01): : 38 - 43
  • [2] FISH SCALES AS BIOSENSORS FOR CATECHOLAMINES
    ELWING, H
    KARLSSON, JOG
    GRUNDSTROM, N
    GUSTAFSSON, ALE
    VONSCHENCK, H
    SUNDGREN, H
    ODMAN, S
    ANDERSSON, RGG
    LUNDSTROM, I
    [J]. BIOSENSORS & BIOELECTRONICS, 1990, 5 (06) : 449 - 459
  • [3] Morphine and morphine-6-glucuronide plasma concentrations and effect in cancer pain
    Faura, CC
    Moore, RA
    Horga, JF
    Hand, CW
    McQuay, HJ
    [J]. JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 1996, 11 (02) : 95 - 102
  • [4] Melatonin-induced organelle movement in melanophores is coupled to tyrosine phosphorylation of a high molecular weight protein
    Karlsson, AM
    Lerner, MR
    Unett, D
    Lundström, I
    Svensson, SPS
    [J]. CELLULAR SIGNALLING, 2000, 12 (07) : 469 - 474
  • [5] THE MELANOPHORE AGGREGATING RESPONSE OF ISOLATED FISH SCALES - A VERY RAPID AND SENSITIVE DIAGNOSIS OF WHOOPING-COUGH
    KARLSSON, JOG
    ANDERSSON, RGG
    ASKELOF, P
    ELWING, H
    GRANSTROM, M
    GRUNDSTROM, N
    LUNDSTROM, I
    OHMAN, L
    [J]. FEMS MICROBIOLOGY LETTERS, 1991, 82 (02) : 169 - 175
  • [6] KOLAKOWSKI LF, 1994, RECEPTOR CHANNEL, V2, P1
  • [7] TOOLS FOR INVESTIGATING FUNCTIONAL INTERACTIONS BETWEEN LIGANDS AND G-PROTEIN-COUPLED RECEPTORS
    LERNER, MR
    [J]. TRENDS IN NEUROSCIENCES, 1994, 17 (04) : 142 - 146
  • [8] Biosensing with G-protein coupled receptor systems
    Lundstrom, I
    Svensson, S
    [J]. BIOSENSORS & BIOELECTRONICS, 1998, 13 (06) : 689 - 695
  • [9] Production of zebrafish germ-line chimeras from embryo cell cultures
    Ma, CG
    Fan, LC
    Ganassin, R
    Bols, N
    Collodi, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) : 2461 - 2466
  • [10] MARTINEZ S, 1999, NEUROSCI INTELL UNIT, V4, P1