Abstract
Megakaryocytes from guinea pig bone marrow were isolated and maintained in liquid culture and were treated with ADP, thrombin, arachidonic acid, or collagen. Megakaryocytes spread with an active ruffled membrane in response to ADP (1-100 microM), thrombin (1.0 U/ml), and arachidonic acid (50 microM) but responded to collagen surfaces only if fibronectin was added to the cultures. Spreading could be blocked completely by dibutyryl cyclic AMP (dibutyryl cAMP) or isobutylmethylxanthine at 1 mM, as well as by cytochalasin D (2 microgram/ml), but not by colchicine up to 1 mg/ml. The distribution of contractile proteins was examined by immunofluorescence. In untreated, spherical cells, staining with antimyosin, antifilamin, anti-alpha- actinin, or with fluorescein-labeled subfragment 1 (FITC-S1) was diffuse and unpatterned. With antitubulin antibody, however, microtubules were seen in a dense array throughout the unspread cells. In actively ruffling spreading cells, myosin, filamin, and actin were visualized in the region of the ruffled membrane while alpha-actinin was seen most prominently in a band located proximal to the inner part of the ruffle. In fully spread cells, actin, myosin, filamin, and alpha- actinin were seen in filaments that filled the cytoplasm. Antimyosin and anti-alpha-actinin staining of the filaments was periodic with approximately 1 micrometer center-to-center spacing. Actin, filamin, and alpha-actinin were also identified in punctate spots throughout the spread cytoplasm. Microtubules were absent from the ruffle but filled the cytoplasm of fully spread cells. Rings, 1.5-2.5 micrometer in diameter, were seen with antitubulin in 13% of the spread cells. Our results show that megakaryocytes respond to platelet agonists, but typically by spreading, rather than extending, filopodia. From the changes in localization of contractile proteins and from time-lapse cinematography, we propose a model for cell spreading.
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- Allen R. D., Zacharski L. R., Widirstky S. T., Rosenstein R., Zaitlin L. M., Burgess D. R. Transformation and motility of human platelets: details of the shape change and release reaction observed by optical and electron microscopy. J Cell Biol. 1979 Oct;83(1):126–142. doi: 10.1083/jcb.83.1.126. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Behnke O. An electron microscope study of the rat megacaryocyte. II. Some aspects of platelet release and microtubules. J Ultrastruct Res. 1969 Jan;26(1):111–129. doi: 10.1016/s0022-5320(69)90039-2. [DOI] [PubMed] [Google Scholar]
- Behnke O., Emmersen J. Structural identification of thrombosthenin in rat megakaryocytes. Scand J Haematol. 1972;9(2):130–137. doi: 10.1111/j.1600-0609.1972.tb00921.x. [DOI] [PubMed] [Google Scholar]
- Behnke O. Microtubules in disk-shaped blood cells. Int Rev Exp Pathol. 1970;9:1–92. [PubMed] [Google Scholar]
- Boyles J., Bainton D. F. Changing patterns of plasma membrane-associated filaments during the initial phases of polymorphonuclear leukocyte adherence. J Cell Biol. 1979 Aug;82(2):347–368. doi: 10.1083/jcb.82.2.347. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brenner S. L., Korn E. D. The effects of cytochalasins on actin polymerization and actin ATPase provide insights into the mechanism of polymerization. J Biol Chem. 1980 Feb 10;255(3):841–844. [PubMed] [Google Scholar]
- Burridge K., McCullough L. The association of alpha-actinin with the plasma membrane. J Supramol Struct. 1980;13(1):53–65. doi: 10.1002/jss.400130106. [DOI] [PubMed] [Google Scholar]
- Condeelis J. S., Taylor D. L. The contractile basis of amoeboid movement. V. The control of gelation, solation, and contraction in extracts from Dictyostelium discoideum. J Cell Biol. 1977 Sep;74(3):901–927. doi: 10.1083/jcb.74.3.901. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Falcão L., Gautier A. Recherches ultrastructurales sur la libération des plaquettes par les mégacaryocytes humains. Blut. 1967 Nov;16(2):57–64. doi: 10.1007/BF01632879. [DOI] [PubMed] [Google Scholar]
- Fallon J. R., Nachmias V. T. Localization of cytoplasmic and skeletal myosins in developing muscle cells by double-label immunofluorescence. J Cell Biol. 1980 Oct;87(1):237–247. doi: 10.1083/jcb.87.1.237. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fedorko M. E. The functional capacity of guinea pig megakaryocytes. I. Uptake of 3H-serotonin by megakaryocytes and their physiologic and morphologic response to stimuli for the platelet release reaction. Lab Invest. 1977 Mar;36(3):310–320. [PubMed] [Google Scholar]
- Fedorko M. E. The functional capacity of guinea pig megakaryocytes. II. The uptake of particles and macromolecules and the effect of rabbit antiguinea pig platelet antiserum. Lab Invest. 1977 Mar;36(3):321–328. [PubMed] [Google Scholar]
- Flanagan M. D., Lin S. Cytochalasins block actin filament elongation by binding to high affinity sites associated with F-actin. J Biol Chem. 1980 Feb 10;255(3):835–838. [PubMed] [Google Scholar]
- Gail M. H., Boone C. W. Effect of colcemid on fibroblast motility. Exp Cell Res. 1971 Mar;65(1):221–227. doi: 10.1016/s0014-4827(71)80070-8. [DOI] [PubMed] [Google Scholar]
- Gonnella P. A., Nachmias V. T. Platelet activation and microfilament bundling. J Cell Biol. 1981 Apr;89(1):146–151. doi: 10.1083/jcb.89.1.146. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grinnell F., Minter D. Attachment and spreading of baby hamster kidney cells to collagen substrata: effects of cold-insoluble globulin. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4408–4412. doi: 10.1073/pnas.75.9.4408. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HUXLEY H. E. ELECTRON MICROSCOPE STUDIES ON THE STRUCTURE OF NATURAL AND SYNTHETIC PROTEIN FILAMENTS FROM STRIATED MUSCLE. J Mol Biol. 1963 Sep;7:281–308. doi: 10.1016/s0022-2836(63)80008-x. [DOI] [PubMed] [Google Scholar]
- Keyserlingk D. G., Albrecht M. Uber die Pseudopodien von Megakaryocyten und ihre Bedeutung für die Freisetzung von Thrombocyten. Z Zellforsch Mikrosk Anat. 1968;89(3):320–327. [PubMed] [Google Scholar]
- Lazarides E. Actin, alpha-actinin, and tropomyosin interaction in the structural organization of actin filaments in nonmuscle cells. J Cell Biol. 1976 Feb;68(2):202–219. doi: 10.1083/jcb.68.2.202. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lazarides E., Burridge K. Alpha-actinin: immunofluorescent localization of a muscle structural protein in nonmuscle cells. Cell. 1975 Nov;6(3):289–298. doi: 10.1016/0092-8674(75)90180-4. [DOI] [PubMed] [Google Scholar]
- Lazarides E., Weber K. Actin antibody: the specific visualization of actin filaments in non-muscle cells. Proc Natl Acad Sci U S A. 1974 Jun;71(6):2268–2272. doi: 10.1073/pnas.71.6.2268. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Levine R. F. Culture in vitro of isolated guinea pig megakaryocytes: recovery, survival, morphologic changes, and maturation. Blood. 1977 Oct;50(4):713–725. [PubMed] [Google Scholar]
- Levine R. F., Fedorko M. E. Isolation of intact megakaryocytes from guinea pig femoral marrow. Successful harvest made possible with inhibitions of platelet aggregation; enrichment achieved with a two-step separation technique. J Cell Biol. 1976 Apr;69(1):159–172. doi: 10.1083/jcb.69.1.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller J. L., Sheridan J. D., White J. G. Electrical responses by guinea pig megakaryocytes. Nature. 1978 Apr 13;272(5654):643–645. doi: 10.1038/272643a0. [DOI] [PubMed] [Google Scholar]
- Nachmias V. T. Cytoskeleton of human platelets at rest and after spreading. J Cell Biol. 1980 Sep;86(3):795–802. doi: 10.1083/jcb.86.3.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Osborn M., Weber K. The display of microtubules in transformed cells. Cell. 1977 Nov;12(3):561–571. doi: 10.1016/0092-8674(77)90257-4. [DOI] [PubMed] [Google Scholar]
- Rabellino E. M., Nachman R. L., Williams N., Winchester R. J., Ross G. D. Human megakaryocytes. I. Characterization of the membrane and cytoplasmic components of isolated marrow megakaryocytes. J Exp Med. 1979 Jun 1;149(6):1273–1287. doi: 10.1084/jem.149.6.1273. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanger J. W. Changing patterns of actin localization during cell division. Proc Natl Acad Sci U S A. 1975 May;72(5):1913–1916. doi: 10.1073/pnas.72.5.1913. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schulz H., Schiller K. Mikrotubuli und Filamente in prospektiven Plättchenfeldern der Megakaryocyten. Z Zellforsch Mikrosk Anat. 1968;87(3):389–400. [PubMed] [Google Scholar]
- Spudich J. A., Watt S. The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin. J Biol Chem. 1971 Aug 10;246(15):4866–4871. [PubMed] [Google Scholar]
- THIERY J. P., BESSIS M. Mécanisme de la plaquettogénèse; etude in vitro par la microcinématographie. Rev Hematol. 1956 Apr-May;11(2):162–174. [PubMed] [Google Scholar]
- Tucker R. W., Sanford K. K., Frankel R. Tubulin and actin in paired nonneoplastic and spontaneously transformed neoplastic cell lines in vitro: fluorescent antibody studies. Cell. 1978 Apr;13(4):629–642. doi: 10.1016/0092-8674(78)90213-1. [DOI] [PubMed] [Google Scholar]
- Wallach D., Davies P., Bechtel P., Willingham M., Pastan I. Cyclic AMP-dependent phosphorylation of the actin-binding protein filamin. Adv Cyclic Nucleotide Res. 1978;9:371–379. [PubMed] [Google Scholar]
- Weber K., Groeschel-Stewart U. Antibody to myosin: the specific visualization of myosin-containing filaments in nonmuscle cells. Proc Natl Acad Sci U S A. 1974 Nov;71(11):4561–4564. doi: 10.1073/pnas.71.11.4561. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weeds A. G., Taylor R. S. Separation of subfragment-1 isoenzymes from rabbit skeletal muscle myosin. Nature. 1975 Sep 4;257(5521):54–56. doi: 10.1038/257054a0. [DOI] [PubMed] [Google Scholar]
- Witkowski J. A., Brighton W. D. Stages of spreading of human diploid cells on glass surfaces. Exp Cell Res. 1971 Oct;68(2):372–380. doi: 10.1016/0014-4827(71)90162-5. [DOI] [PubMed] [Google Scholar]
