Literature DB >> 791737

Cellular interrelationships during in vitro granulopoiesis.

T D Allen, T M Dexter.   

Abstract

Long-term production of fully differentiated granulocytes can be maintained in vitro in a liquid system of cultured bone marrow. Marrow is cultured in medical flasks and allowed to form an adherent layer over a three-week period, and then recharged with fresh marrow resulting in continued mature granulocyte production for several months. During the initial establishment of the adherent layer, three attached populations become apparent: phagocytic monocytes, an attached epithelial cell type, and aggregations of epithelial cells swollen to enormous proportions by the presence of numerous lipid-containing vacuoles. Without the formation of these aggregations, granulocyte production is not maintained beyond an initial period and the culture converts to phagocytic mononuclear cell production alone. Thus not only is the presence of the fat-containing aggregations necessary to continued granulopoiesis, but cultures in full granulocyte production show a characteristic clumping of granulocytes around these aggregates. Electron microscopy has shown that the epithelial cells from the adherent layer form a layer covering some of the attached cells in these areas and thus may provide the necessary in vitro microenvironment for granulopoiesis to occur. Pinocytotic vesicles and gap junctions have been observed between the adjacent membranes of the undifferentiated granulocytes (possibly stem cells) and the epithelial cells themselves.

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Year:  1976        PMID: 791737     DOI: 10.1111/j.1432-0436.1976.tb01486.x

Source DB:  PubMed          Journal:  Differentiation        ISSN: 0301-4681            Impact factor:   3.880


  21 in total

1.  Multinucleated giant cells in primary cultures derived from canine bone marrow--evidence for formation of putative osteoclasts.

Authors:  M C Bird; D Garside; H B Jones
Journal:  Cell Tissue Res       Date:  1992-04       Impact factor: 5.249

2.  Tissue-specific inhibitor of lymphocyte proliferation extracted and purified from calf spleen. Biological and chemical properties.

Authors:  E Heidemann; N Podgornik; K Wilms
Journal:  Blut       Date:  1979-10

Review 3.  Stromal cells and stem cells in clinical bone regeneration.

Authors:  Warren L Grayson; Bruce A Bunnell; Elizabeth Martin; Trivia Frazier; Ben P Hung; Jeffrey M Gimble
Journal:  Nat Rev Endocrinol       Date:  2015-01-06       Impact factor: 43.330

4.  Immunochemical characterization and ultrastructural localization of chondroitin sulfates and keratan sulfate in embryonic chick bone marrow.

Authors:  J M Sorrell; F Mahmoodian; B Caterson
Journal:  Cell Tissue Res       Date:  1988-06       Impact factor: 5.249

5.  In vitro homing of hemopoietic stem cells is mediated by a recognition system with galactosyl and mannosyl specificities.

Authors:  S Aizawa; M Tavassoli
Journal:  Proc Natl Acad Sci U S A       Date:  1987-07       Impact factor: 11.205

6.  The Ets-related transcription factor PU.1 immortalizes erythroblasts.

Authors:  S Schuetze; P E Stenberg; D Kabat
Journal:  Mol Cell Biol       Date:  1993-09       Impact factor: 4.272

7.  Morphologic analysis of long-term bone marrow cultures that support B-lymphopoiesis or myelopoiesis.

Authors:  K Dorshkind; L Schouest; W H Fletcher
Journal:  Cell Tissue Res       Date:  1985       Impact factor: 5.249

8.  Myelo-lymphopoiesis in long-term bone marrow culture.

Authors:  H G Mergenthaler
Journal:  Klin Wochenschr       Date:  1985-04-15

9.  Cellular aggregates in bone marrow cultures of patients with acute myeloid leukemia.

Authors:  R E Merchant; M R Müller
Journal:  Blut       Date:  1982-06

10.  Murine bone marrow cell line producing colony-stimulating factor.

Authors:  K Harigaya; E P Cronkite; M E Miller; R K Shadduck
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

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