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. 1977 Aug 1;74(2):351–357. doi: 10.1083/jcb.74.2.351

Physiological regulation of total tubulin and polymerized tubulin in tissues

PMCID: PMC2110064  PMID: 328515

Abstract

Polymerized and depolymerized forms of tubulin were measured in rat and mouse liver, rat islets, human lymphocytes, and platelets. The percent of the total tubulin present in the polymerized form varied from 30.3 +/- 1.5% in the liver of the fed rat to 89.2 +/- 0.2% in human platelets. Fasting decreased the total tubulin and to a greater extent the polymerized form of tubulin in both rat and mouse liver. Glucose feeding increased the polymerized tubulin without affecting the total tubulin content in rat liver. Phytohemagglutinin-stimulated lymphocytes exhibited at least a three-fold increase in total tubulin (expressed in terms of DNA content), which during the initial 48 h of incubation was accounted for in toto by an increase in polymerized tubulin. It is suggested that the lectin not only accelerates tubulin synthesis but also stimulated the polymerization process. Storage of platelets at 4 degrees C for 6 days resulted in a marked decrease in total tubulin and an even greater reduction in the polymerized form. It is concluded that both the total tubulin content and its degree of polymerization can be modulated independently by a wide variety of physiological factors.

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Selected References

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  1. Dahlström A. Effect of colchicine on transport of amine storage granules in sympathetic nerves of rat. Eur J Pharmacol. 1968 Dec;5(1):111–113. doi: 10.1016/0014-2999(68)90165-9. [DOI] [PubMed] [Google Scholar]
  2. Eaton R. P., Kipnis D. M. Effect of glucose feeding on lipoprotein synthesis in the rat. Am J Physiol. 1969 Oct;217(4):1153–1159. doi: 10.1152/ajplegacy.1969.217.4.1153. [DOI] [PubMed] [Google Scholar]
  3. Eaton R. P., Kipnis D. M., Karl I., Eisenstein A. B. Effects of glucose feeding on insulin and glucagon secretion and hepatic gluconeogenesis in the rat. Am J Physiol. 1974 Jul;227(1):101–104. doi: 10.1152/ajplegacy.1974.227.1.101. [DOI] [PubMed] [Google Scholar]
  4. Friedman F., Detwiler T. C. Stimulus-secretion coupling in platelets. Effects of drugs on secretion on adenosine 5'-triphosphate. Biochemistry. 1975 Mar 25;14(6):1315–1320. doi: 10.1021/bi00677a033. [DOI] [PubMed] [Google Scholar]
  5. Gillespie E., Levine R. J., Malawista S. E. Histamine release from rat peritoneal mast cells: inhibition by colchicine and potentiation by deuterium oxide. J Pharmacol Exp Ther. 1968 Nov;164(1):158–165. [PubMed] [Google Scholar]
  6. HEIMBERG M., WEINSTEIN I., KLAUSNER H., WATKINS M. L. Release and uptake of triglycerides by isolated perfused rat liver. Am J Physiol. 1962 Feb;202:353–358. doi: 10.1152/ajplegacy.1962.202.2.353. [DOI] [PubMed] [Google Scholar]
  7. KISSANE J. M., ROBINS E. The fluorometric measurement of deoxyribonucleic acid in animal tissues with special reference to the central nervous system. J Biol Chem. 1958 Jul;233(1):184–188. [PubMed] [Google Scholar]
  8. Kirschner M. W., Williams R. C., Weingarten M., Gerhart J. C. Microtubules from mammalian brain: some properties of their depolymerization products and a proposed mechanism of assembly and disassembly. Proc Natl Acad Sci U S A. 1974 Apr;71(4):1159–1163. doi: 10.1073/pnas.71.4.1159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kowit J. D., Fulton C. Programmed synthesis of tubulin for the flagella that develop during cell differentiation in Naegleria gruberi. Proc Natl Acad Sci U S A. 1974 Jul;71(7):2877–2881. doi: 10.1073/pnas.71.7.2877. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  11. Lacy P. E., Howell S. L., Young D. A., Fink C. J. New hypothesis of insulin secretion. Nature. 1968 Sep 14;219(5159):1177–1179. doi: 10.1038/2191177a0. [DOI] [PubMed] [Google Scholar]
  12. Le Marchand Y., Singh A., Assimacopoulos-Jeannet F., Orci L., Rouiller C., Jeanrenaud B. A role for the microtubular system in the release of very low density lipoproteins by perfused mouse livers. J Biol Chem. 1973 Oct 10;248(19):6862–6870. [PubMed] [Google Scholar]
  13. MALAWISTA S. E. ON THE ACTION OF COLCHICINE, THE MELANOCYTE MODEL. J Exp Med. 1965 Aug 1;122:361–384. doi: 10.1084/jem.122.2.361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Murphy S., Gardner F. H. Effect of storage temperature on maintenance of platelet viability--deleterious effect of refrigerated storage. N Engl J Med. 1969 May 15;280(20):1094–1098. doi: 10.1056/NEJM196905152802004. [DOI] [PubMed] [Google Scholar]
  15. Oliver J. M., Ukena T. E., Berlin R. D. Effects of phagocytosis and colchicine on the distribution of lectin-binding sites on cell surfaces. Proc Natl Acad Sci U S A. 1974 Feb;71(2):394–398. doi: 10.1073/pnas.71.2.394. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Olmsted J. B., Borisy G. G. Microtubules. Annu Rev Biochem. 1973;42:507–540. doi: 10.1146/annurev.bi.42.070173.002451. [DOI] [PubMed] [Google Scholar]
  17. Pipeleers D. G., Pipeleers-Marichal M. A., Kipnis D. M. Microtubule assembly and the intracellular transport of secretory granules in pancreatic islets. Science. 1976 Jan 9;191(4222):88–90. doi: 10.1126/science.1108194. [DOI] [PubMed] [Google Scholar]
  18. Pipeleers D. G., Pipeleers-Marichal M. A., Sherline P., Kipnis D. M. A sensitive method for measuring polymerized and depolymerized forms of tubulin in tissues. J Cell Biol. 1977 Aug;74(2):341–350. doi: 10.1083/jcb.74.2.341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Quarfordt S. H., Frank A., Shames D. M., Berman M., Steinberg D. Very low density lipoprotein triglyceride transport in type IV hyperlipoproteinemia and the effects of carbohydrate-rich diets. J Clin Invest. 1970 Dec;49(12):2281–2297. doi: 10.1172/JCI106448. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Reaven E. P., Reaven G. M. A quantitative ultrastructural study of microtubule content and secretory granule accumulation in parathyroid glands of phosphate- and colchicine-treated rats. J Clin Invest. 1975 Jul;56(1):49–55. doi: 10.1172/JCI108078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Shelanski M. L., Gaskin F., Cantor C. R. Microtubule assembly in the absence of added nucleotides. Proc Natl Acad Sci U S A. 1973 Mar;70(3):765–768. doi: 10.1073/pnas.70.3.765. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Smith J. W., Steiner A. L., Parker C. W. Human lymphocytic metabolism. Effects of cyclic and noncyclic nucleotides on stimulation by phytohemagglutinin. J Clin Invest. 1971 Feb;50(2):442–448. doi: 10.1172/JCI106511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Stein O., Sanger L., Stein Y. Colchicine-induced inhibition of lipoprotein and protein secretion into the serum and lack of interference with secretion of biliary phospholipids and cholesterol by rat liver in vivo. J Cell Biol. 1974 Jul;62(1):90–103. doi: 10.1083/jcb.62.1.90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Tilney L. G. Studies on the microtubules in heliozoa. IV. The effect of colchicine on the formation and maintenance of the axopodia and the redevelopment of pattern in Actinosphaerium nucleofilum (Barrett). J Cell Sci. 1968 Dec;3(4):549–562. doi: 10.1242/jcs.3.4.549. [DOI] [PubMed] [Google Scholar]
  25. Tollefsen D. M., Feagler J. R., Majerus P. W. Induction of the platelet release reaction by phytohemagglutinin. J Clin Invest. 1974 Jan;53(1):211–218. doi: 10.1172/JCI107540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Weingarten M. D., Lockwood A. H., Hwo S. Y., Kirschner M. W. A protein factor essential for microtubule assembly. Proc Natl Acad Sci U S A. 1975 May;72(5):1858–1862. doi: 10.1073/pnas.72.5.1858. [DOI] [PMC free article] [PubMed] [Google Scholar]

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