Literature DB >> 9216740

Localization of megakaryocytes in normal mice and following administration of platelet antiserum, 5-fluorouracil, or radiostrontium: evidence for the site of platelet production.

R E Davis1, P E Stenberg, J Levin, J H Beckstead.   

Abstract

The relative contributions of various organs to platelet production is controversial. In this study, serial histologic sections of bone marrow, spleen, liver, and lung from normal C57BL/6J mice and mice that had received three different agents which perturb normal murine thrombopoiesis (platelet antiserum, 5-fluorouracil, and radioactive strontium) were examined for the presence of megakaryocytes, utilizing morphologic and immunohistochemical techniques for their identification. In liver and lung tissue, megakaryocytes (including their naked nuclei or large cytoplasmic fragments) were rare in whole cross-sections (which included blood vessels) from normal and perturbed mice, even during periods of strong stimulation of thrombopoiesis. In contrast, megakaryocyte numbers were greatly increased in bone marrow and/or spleen tissue in these circumstances. We conclude that: 1) the bone marrow and spleen are the major thrombopoietic organs in the mouse, and 2) an insignificant fraction of thrombocytopoiesis occurs in the murine liver or lung, even during periods of greatly increased platelet production or following loss of the spleen and/or bone marrow.

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Year:  1997        PMID: 9216740

Source DB:  PubMed          Journal:  Exp Hematol        ISSN: 0301-472X            Impact factor:   3.084


  14 in total

1.  Platelet production in the pulmonary capillary bed: new ultrastructural evidence for an old concept.

Authors:  D Zucker-Franklin; C S Philipp
Journal:  Am J Pathol       Date:  2000-07       Impact factor: 4.307

Review 2.  Does size matter in platelet production?

Authors:  Jonathan N Thon; Joseph E Italiano
Journal:  Blood       Date:  2012-06-04       Impact factor: 22.113

Review 3.  In vivo platelet production from mature megakaryocytes: does platelet release occur via proplatelets?

Authors:  Goro Kosaki
Journal:  Int J Hematol       Date:  2005-04       Impact factor: 2.490

4.  Visualization of microtubule growth in living platelets reveals a dynamic marginal band with multiple microtubules.

Authors:  Sunita Patel-Hett; Jennifer L Richardson; Harald Schulze; Ksenija Drabek; Natasha A Isaac; Karin Hoffmeister; Ramesh A Shivdasani; J Chloë Bulinski; Niels Galjart; John H Hartwig; Joseph E Italiano
Journal:  Blood       Date:  2008-01-29       Impact factor: 22.113

5.  Mutational inhibition of c-Myb or p300 ameliorates treatment-induced thrombocytopenia.

Authors:  Douglas J Hilton; Benjamin T Kile; Warren S Alexander
Journal:  Blood       Date:  2009-02-27       Impact factor: 22.113

Review 6.  Platelet Biogenesis in the Lung Circulation.

Authors:  Emma Lefrançais; Mark R Looney
Journal:  Physiology (Bethesda)       Date:  2019-11-01

7.  Megakaryocyte migration defects due to nonmuscle myosin IIA mutations underlie thrombocytopenia in MYH9-related disease.

Authors:  Kasturi Pal; Roberta Nowak; Neil Billington; Rong Liu; Arit Ghosh; James R Sellers; Velia M Fowler
Journal:  Blood       Date:  2020-05-21       Impact factor: 22.113

8.  A study of P2X1 receptor function in murine megakaryocytes and human platelets reveals synergy with P2Y receptors.

Authors:  Catherine Vial; Michael G Rolf; Martyn P Mahaut-Smith; Richard J Evans
Journal:  Br J Pharmacol       Date:  2002-01       Impact factor: 8.739

Review 9.  Platelets in lung biology.

Authors:  Andrew S Weyrich; Guy A Zimmerman
Journal:  Annu Rev Physiol       Date:  2012-10-01       Impact factor: 19.318

10.  Transendothelial migration of megakaryocytes in response to stromal cell-derived factor 1 (SDF-1) enhances platelet formation.

Authors:  T Hamada; R Möhle; J Hesselgesser; J Hoxie; R L Nachman; M A Moore; S Rafii
Journal:  J Exp Med       Date:  1998-08-03       Impact factor: 14.307

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