Rheological properties of living cytoplasm: endoplasm of Physarum plasmodium.
Open Access
- 1 October 1983
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 97 (4), 1089-1097
- https://doi.org/10.1083/jcb.97.4.1089
Abstract
Magnetic sphere viscoelastometry, video microscopy, and the Kamiya double chamber method (Kamiya, N., 1940, Science [Wash. DC], 92:462-463.) have been combined in an optical and rheological investigation of the living endoplasm of Physarum polycephalum. The rheological properties examined were yield stress, viscosity (as a function of shear), and elasticity. These parameters were evaluated in directions perpendicular; (X) and parallel (Y) to the plasmodial vein. Known magnetic forces were used for measurements in the X direction, while the falling ball technique was used in the Y direction (Cygan, D.A., and B. Caswell, 1971, Trans. Soc. Rheol. 15:663-683; MacLean-Fletcher, S.D., and T.D. Pollard, 1980, J. Cell Biol., 85:414-428). Approximate yield stresses were calculated in the X and Y directions of 0.58 and 1.05 dyn/cm2, respectively. Apparent viscosities measured in the two directions (eta x and eta y) were found to fluctuate with time. The fluctuations in eta x and eta y were shown, statistically, to occur independently of each other. Frequency correlation with dynamoplasmograms indicated that these fluctuations probably occur independently of the streaming cycle. Viscosity was found to be a complex function of shear, indicating that the endoplasm is non-Newtonian. Plots of shear stress vs. rate of shear both parallel and perpendicular to the vein, showed that endoplasm is not a shear thinning material. These experiments have shown that living endoplasm of Physarum is an anisotropic viscoelastic fluid with a yield stress. The endoplasm appears not to be a homogeneous material, but to be composed of heterogeneous domains.Keywords
This publication has 30 references indexed in Scilit:
- Video‐enhanced microscopy with a computer frame memoryJournal of Microscopy, 1983
- A novel 36,000-dalton actin-binding protein purified from microfilaments in Physarum plasmodia which aggregates actin filaments and blocks actin-myosin interaction.The Journal of cell biology, 1982
- Plasmalemma invaginations of Physarum dependent on the nutritional content of the plasmodial environmentJournal of Cell Science, 1979
- Transformation of cytoplasmic actin importance for the organization of the contractile gel reticulnm and the contraction ? relaxation cycle of cytoplasmic actomyosinCell and tissue research, 1976
- Rheology of F-actin I. Network of F-actin in solutionBiochimica et Biophysica Acta (BBA) - Protein Structure, 1974
- [13] Flow birefringenceMethods in Enzymology, 1972
- THE CHANGING PATTERN OF BIREFRINGENCE IN PLASMODIA OF THE SLIME MOLD, PHYSARUM POLYCEPHALUM The Journal of cell biology, 1965
- The mechanical and colloidal properties of Amoeba protoplasm and their relations to the mechanism of amoeboid movementComparative Biochemistry and Physiology, 1961
- THE CONSISTENCY OF AMEBA CYTOPLASM AND ITS BEARING ON THE MECHANISM OF AMEBOID MOVEMENTThe Journal of cell biology, 1960
- The Control of Protoplasmic StreamingScience, 1940