Literature DB >> 6255979

Ultrastructural studies of erythropoiesis in beta-thalassaemia trait.

S N Wickramasinghe, M Hughes.   

Abstract

The erythropoietic cells of six cases of beta-thalassaemia trait were studied by electron microscopy and electron microscope autoradiography. Intracytoplasmic and intranuclear alpha-chain precipitates were found in some late polychromatic erythroblasts and intracytoplasmic precipitates were found in several marrow reticulocytes. This provides direct morphological evidence of unbalanced globin chain synthesis in the marrow. Several of the polychromatic erythroblasts and marrow reticulocytes contained autophagic vacuoles and showed a variety of other dyserythropoietic changes. Erythroblast profiles containing moderate quantities of precipitated alpha-chains usually suffered from a marked depression of protein synthesis. The proportions of marrow cells containing alpha-chain precipitates and displaying dyserythropoietic changes varied considerably from patient to patient. It is proposed that this variation largely reflects variations in the proteolytic capacity of the erythropoietic cells in different individuals and leads to different degrees of ineffective erythropoiesis in beta-thalassaemia trait.

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Year:  1980        PMID: 6255979     DOI: 10.1111/j.1365-2141.1980.tb05986.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  5 in total

Review 1.  Protein quality control during erythropoiesis and hemoglobin synthesis.

Authors:  Eugene Khandros; Mitchell J Weiss
Journal:  Hematol Oncol Clin North Am       Date:  2010-12       Impact factor: 3.722

2.  Studies of erythroblast function in congenital dyserythropoietic anaemia, type I: evidence of impaired DNA, RNA, and protein synthesis and unbalanced globin chain synthesis in ultrastructurally abnormal cells.

Authors:  S N Wickramasinghe; M J Pippard
Journal:  J Clin Pathol       Date:  1986-08       Impact factor: 3.411

3.  Integrated protein quality-control pathways regulate free α-globin in murine β-thalassemia.

Authors:  Eugene Khandros; Christopher S Thom; Janine D'Souza; Mitchell J Weiss
Journal:  Blood       Date:  2012-03-16       Impact factor: 22.113

4.  The autophagy-activating kinase ULK1 mediates clearance of free α-globin in β-thalassemia.

Authors:  Christophe Lechauve; Julia Keith; Eugene Khandros; Stephanie Fowler; Kalin Mayberry; Abdullah Freiwan; Christopher S Thom; Paola Delbini; Emilio Boada Romero; Jingjing Zhang; Irene Motta; Heather Tillman; M Domenica Cappellini; Mondira Kundu; Mitchell J Weiss
Journal:  Sci Transl Med       Date:  2019-08-21       Impact factor: 17.956

5.  A new case of congenital dyserythropoietic anaemia, type III: studies of the cell cycle distribution and ultrastructure of erythroblasts and of nucleic acid synthesis in marrow cells.

Authors:  S N Wickramasinghe; T E Parry; C Williams; A N Bond; M Hughes; S Crook
Journal:  J Clin Pathol       Date:  1982-10       Impact factor: 3.411

  5 in total

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