Literature DB >> 2908867

Differential location of hemopoietic colonies within liver acini of postnatal and phenylhydrazine-treated adult mice.

E Barberá-Guillem1, R Ayala, F Vidal-Vanaclocha.   

Abstract

We have measured the location of embryonic and adult hemopoietic foci in the liver tissue of postnatal and adult phenylhydrazine-treated mice. Differentiation of acinar domains in liver tissue was made possible by carrying out succinate dehydrogenase histochemical reactions on liver cryostat sections. To determine the position of hemopoietic foci within the lobular gradient of the hepatocyte succinate dehydrogenase activity, this enzyme was measured in hepatocytes surrounding both portal and central veins and hemopoietic foci. Then, assuming the periportal succinate dehydrogenase activity value to be 1.00 +/- 0.2, succinate dehydrogenase activity around postnatal hemopoietic foci was 0.65 +/- 0.19, around phenylhydrazine-induced hemopoietic foci 0.83 +/- 0.24 and around central veins 0.44 +/- 0.11. Scaling the portal to central vein distance and taking 1 as the portal vein point and 0 as the central vein point, the relative position of hemopoietic foci, indirectly calculated from succinate dehydrogenase activity values, was 0.35 +/- 0.13 in postnatal livers and 0.73 +/- 0.12 in phenylhydrazine-treated adult livers. Hemopoietic foci frequencies varied according to both the origin and the liver acinar domain: in postnatal liver acini, it was 37.1% in zone 1, 22.8% in zone 2 and 40% in zone 3; in phenylhydrazine-treated adult acini, it was 89.4% in zone 1 and 10.6% in zone 2. Postnatal hemopoietic foci mainly occurred extrasinusoidally, between hepatocytes and reticular-like cells, whereas adult hemopoietic foci were mostly intrasinusoidal and closely associated to macrophage-like cells. Adult hemopoietic colonies

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Year:  1989        PMID: 2908867     DOI: 10.1002/hep.1840090106

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  4 in total

1.  Functional variations in liver tissue during the implantation process of metastatic tumour cells.

Authors:  F Vidal-Vanaclocha; A Alonso-Varona; R Ayala; E Barberá-Guillem
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

2.  Biliary Epithelial Cells Are Not the Predominant Source of Hepatic CXCL12.

Authors:  Yedidya Saiman; Tatsuki Sugiyama; Noa Simchoni; Carlo Spirli; Meena B Bansal
Journal:  Am J Pathol       Date:  2015-04-29       Impact factor: 4.307

3.  Extramedullary erythropoiesis in the adult liver requires BMP-4/Smad5-dependent signaling.

Authors:  Laurie E Lenox; Lei Shi; Shailaja Hegde; Robert F Paulson
Journal:  Exp Hematol       Date:  2009-05       Impact factor: 3.084

4.  The prometastatic microenvironment of the liver.

Authors:  Fernando Vidal-Vanaclocha
Journal:  Cancer Microenviron       Date:  2008-05-17
  4 in total

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