Literature DB >> 8751107

Histocytochemical and immunohistochemical studies related to the role of glycogen in human developing digestive organs.

K Hashimoto1, K Tamura, H Otani, O Tanaka.   

Abstract

To elucidate the role of glycogen in the epithelium of developing digestive organs, we investigated the appearance of glycogen and glycogen phosphorylase (GP) in these organs. We studied 64 externally normal human embryos at Carnegie stages 13-23 (5.1-28.0 mm in crown-rump length, 4-8 weeks of gestation) by histocytochemical staining for glycogen and immunohistochemical staining with antibodies against two isoenzymes of GP: brain-type (BGP) and muscle-brain-type (MBGP) GP. At stage 13, glycogen appeared in the epithelium of the digestive tract and the parenchyma of the pancreas. As development advanced, glycogen granules increased in number and size in these tissues, and they became evenly distributed in the epithelium of the digestive tract as either single particles or aggregates, as deduced by electron microscopy at late embryonic stages. Immunoreactivity specific both for BGP and for MBGP was detected in the digestive tract and the pancreas from stage 13. As development advanced, both BGP- and MBGP-immunoreactive cells increased in number and in immunoreactivity, and the number of MBGP-immunoreactive cells became larger than that of BGP-immunoreactive cells. By contrast, in hepatic cells, which serve as a major storage site for glycogen in adults, glycogen was detected only from stage 20, in smaller amounts, without formation of aggregates, and no immunoreactivity specific for BGP or MBGP was apparent throughout the embryonic stages examined. Thus, in the epithelium of the digestive tract and the parenchyma of the pancreas, but not in hepatic cells, the appearance and localization of GP coincided almost exactly with that of glycogen. These observations suggest that glycogen in the epithelium of the digestive tract and the parenchyma of the pancreas has not only been synthesized but also degraded from an early embryonic period and may, thus, be related to active cellular metabolism that is specific for embryonic development, including proliferation of the epithelium and interactions between epithelium and mesenchyme.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8751107     DOI: 10.1007/bf00187180

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  39 in total

1.  The intermediary metabolism of human fetal tissues.

Authors:  C A VILLEE
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1954

2.  A microchemical reaction resulting in the staining of polysaccharide structures in fixed tissue preparations.

Authors:  R D HOTCHKISS
Journal:  Arch Biochem       Date:  1948-01

Review 3.  [Carcinofetal alterations in isozymes, with special reference to glycogen phosphorylase (author's transl)].

Authors:  K Sato
Journal:  Seikagaku       Date:  1977-10

4.  Influence of hormones on glycogen and glucose metabolism in embryonic chick intestine.

Authors:  B L Black
Journal:  Am J Physiol       Date:  1988-01

5.  Guide to the staging of human embryos.

Authors:  R O'Rahilly
Journal:  Anat Anz       Date:  1972

6.  Normal and abnormal development of human embryos: first report of the analysis of 1,213 intact embryos.

Authors:  H Nishimura; K Takano; T Tanimura; M Yasuda
Journal:  Teratology       Date:  1968-08

7.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.

Authors:  S M Hsu; L Raine; H Fanger
Journal:  J Histochem Cytochem       Date:  1981-04       Impact factor: 2.479

8.  Development of the notochord in human embryos: ultrastructural, histochemical, and immunohistochemical studies.

Authors:  H Shinohara; O Tanaka
Journal:  Anat Rec       Date:  1988-02

9.  The "solid stage" and congenital intestinal atresia.

Authors:  C Moutsouris
Journal:  J Pediatr Surg       Date:  1966-10       Impact factor: 2.545

10.  The structure and deposition of human-liver glycogens.

Authors:  E J Bourne; A McLean; J B Pridham
Journal:  Biochem J       Date:  1966-03       Impact factor: 3.857

View more
  4 in total

1.  Global gene expression profiling and histochemical analysis of the developing human fetal pancreas.

Authors:  S A Sarkar; S Kobberup; R Wong; A D Lopez; N Quayum; T Still; A Kutchma; J N Jensen; R Gianani; G M Beattie; J Jensen; A Hayek; J C Hutton
Journal:  Diabetologia       Date:  2007-12-18       Impact factor: 10.122

2.  Renal expression of the brain and muscle isoforms of glycogen phosphorylase in different cell types.

Authors:  Heide Schmid; Benedikt Dolderer; Ulrike Thiess; Stephan Verleysdonk; Bernd Hamprecht
Journal:  Neurochem Res       Date:  2008-03-13       Impact factor: 3.996

3.  Expression of the brain and muscle isoforms of glycogen phosphorylase in rat heart.

Authors:  Heide Schmid; Brigitte Pfeiffer-Guglielmi; Benedikt Dolderer; Ulrike Thiess; Stephan Verleysdonk; Bernd Hamprecht
Journal:  Neurochem Res       Date:  2008-08-27       Impact factor: 3.996

4.  KIAA1199 interacts with glycogen phosphorylase kinase β-subunit (PHKB) to promote glycogen breakdown and cancer cell survival.

Authors:  Masato Terashima; Yoshihiko Fujita; Yosuke Togashi; Kazuko Sakai; Marco A De Velasco; Shuta Tomida; Kazuto Nishio
Journal:  Oncotarget       Date:  2014-08-30
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.