Literature DB >> 512628

Calcium distribution in Amoeba proteus.

R D Prusch, J A Hannafin.   

Abstract

A preliminary investigation of the distribution of cellular calcium in Amoeba proteus was undertaken. Total cellular calcium under control conditions was found to be 4.59 mmol/kg of cells. When the external Ca++ concentration is increased from the control level of 0.03 to 20 mM, a net Ca++ influx results with a new steady-state cellular calcium level being achieved in integral of 3 h. At steady state the amount of calcium per unit weight of cells is higher than the amount of calcium per unit weight of external solution when the external concentration of Ca++ is below 10 mM. At external Ca++ concentrations above this level, total cellular calcium approaches the medium level of Ca++. Steady-state calcium exchange in Amoeba proteus was determined with 45Ca. There is an immediate and rapid exchange of integral of 0.84 mmol/kg of cells or 18% of the total cellular calcium with the labelled Ca++. Following this initial exchange, there was very little if any further exchange observed. Most of this exchanged calcium could be eliminated from the cell with 1 mM La+++, suggesting that the exchanged calcium is associated with the surface of the cell. Increase in either the external Ca++ concentration of pH raise the amount of exchangeable calcium associated with the cell. Calcium may be associated with the cell surface as a co-ion in the diffuse double layer or bound to fixed negative sites on the surface of the cell. If Ca++-binding sites do exist on the cell surface, there may be more than one type and they may have different dissociation constants. The cytoplasmic Ca++ ion activity is probably maintained at very low levels.

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Year:  1979        PMID: 512628      PMCID: PMC2228564          DOI: 10.1085/jgp.74.4.511

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  3 in total

1.  Pinocytosis and locomotion of amoebae. XV. Visualization of Ca++-dynamics by chlorotetracycline (CTC) fluorescence during induced pinocytosis in living Amoeba proteus.

Authors:  W Gawlitta; W Stockem; J Wehland; K Weber
Journal:  Cell Tissue Res       Date:  1980       Impact factor: 5.249

2.  Contractile basis of ameboid movement. VII. Aequorin luminescence during ameboid movement, endocytosis, and capping.

Authors:  D L Taylor; J R Blinks; G Reynolds
Journal:  J Cell Biol       Date:  1980-08       Impact factor: 10.539

3.  Sucrose uptake by pinocytosis in Amoeba proteus and the influence of external calcium.

Authors:  R D Prusch; J A Hannafin
Journal:  J Gen Physiol       Date:  1979-10       Impact factor: 4.086

  3 in total

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