Literature DB >> 7551349

Ultrastructural changes in the lung in Niemann-Pick type C mouse.

T Manabe1, T Yamane, Y Higashi, P G Pentchev, K Suzuki.   

Abstract

The biochemical and morphological aspects of BALB/c mice with many features of the Niemann-Pick disease type C in man (NP-C mouse) have been studied extensively. However, the pulmonary pathology has not been studied extensively and we describe here some unique ultrastructural features of the lung in the NP-C mouse. Ultrastructurally, macrophages in younger mice contained osmiophilic dense granules and annulolamellar structures, but larger multilamellar concentric structures increased in the macrophages of older mice. In contrast, endothelial cells and type I pneumocytes showed membrane-bound bodies with dense granules and vesicular or vesiculogranular structures as well as amorphous materials. Type II pneumocytes were unremarkable throughout. Our study suggests that endothelial cells and type I pneumocytes are the major site of metabolic derangement resulting in pronounced morphological changes with granular and round membranous structures in the lungs of NP-C mouse. Alveolar macrophages with multilamellar concentric structures may be a result of disturbed disposal of surfactant material from type II pneumocytes rather than that from storage material of type I pneumocyte.

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Year:  1995        PMID: 7551349     DOI: 10.1007/bf00203741

Source DB:  PubMed          Journal:  Virchows Arch        ISSN: 0945-6317            Impact factor:   4.064


  12 in total

1.  Type C Niemann-Pick disease. Lysosomal accumulation and defective intracellular mobilization of low density lipoprotein cholesterol.

Authors:  J Sokol; J Blanchette-Mackie; H S Kruth; N K Dwyer; L M Amende; J D Butler; E Robinson; S Patel; R O Brady; M E Comly
Journal:  J Biol Chem       Date:  1988-03-05       Impact factor: 5.157

2.  Ultrastructural and enzyme histochemical study of liver in Niemann-Pick disease.

Authors:  A Chamlian; J M Gulian; L Benkoël
Journal:  Cell Mol Biol       Date:  1986       Impact factor: 1.770

3.  Freeze-fracture study of alveolar lining layer in adult rat lungs.

Authors:  T Manabe
Journal:  J Ultrastruct Res       Date:  1979-10

4.  Lysosome lipid storage disorder in NCTR-BALB/c mice. II. Morphologic and cytochemical studies.

Authors:  H Shio; S Fowler; C Bhuvaneswaran; M D Morris
Journal:  Am J Pathol       Date:  1982-08       Impact factor: 4.307

5.  Niemann-Pick disease--type C. Ocular histopathologic and electron microscopic studies.

Authors:  M Palmer; W R Green; I H Maumenee; D L Valle; H S Singer; S J Morton; H W Moser
Journal:  Arch Ophthalmol       Date:  1985-06

6.  Fetal Niemann-Pick disease type C: ultrastructural and lipid findings in liver and spleen.

Authors:  C Dumontel; C Girod; F Dijoud; Y Dumez; M T Vanier
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

7.  A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidase.

Authors:  P G Pentchev; A E Gal; A D Booth; F Omodeo-Sale; J Fouks; B A Neumeyer; J M Quirk; G Dawson; R O Brady
Journal:  Biochim Biophys Acta       Date:  1980-09-08

8.  Cerebellar involvement in murine sphingomyelinosis: a new model of Niemann-Pick disease.

Authors:  J Tanaka; H Nakamura; S Miyawaki
Journal:  J Neuropathol Exp Neurol       Date:  1988-05       Impact factor: 3.685

9.  Cerebellar degeneration in the Niemann-Pick type C mouse.

Authors:  Y Higashi; S Murayama; P G Pentchev; K Suzuki
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

10.  Liver findings in Niemann-Pick disease type C.

Authors:  M Elleder; F Smíd; H Hyniová; J Cihula; J Zeman; M Macek
Journal:  Histochem J       Date:  1984-11
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  6 in total

1.  Lysosome lipid storage disorder in NCTR-BALB/c mice: spleen and lung lysosomes store unesterified cholesterol but differ in their phospholipid composition.

Authors:  C Bhuvaneswaran; M D Morris
Journal:  Mol Cell Biochem       Date:  2000-11       Impact factor: 3.396

2.  Ontogenic changes in lung cholesterol metabolism, lipid content, and histology in mice with Niemann-Pick type C disease.

Authors:  Charina M Ramirez; Adam M Lopez; Lam Q Le; Kenneth S Posey; Arthur G Weinberg; Stephen D Turley
Journal:  Biochim Biophys Acta       Date:  2013-09-26

3.  Pulmonary function and pathology in hydroxypropyl-beta-cyclodextin-treated and untreated Npc1⁻/⁻ mice.

Authors:  Akshay Muralidhar; Ivan A Borbon; Dyadin M Esharif; Wangjing Ke; Rinu Manacheril; Michael Daines; Robert P Erickson
Journal:  Mol Genet Metab       Date:  2011-03-05       Impact factor: 4.797

4.  Cyclodextrin overcomes the transport defect in nearly every organ of NPC1 mice leading to excretion of sequestered cholesterol as bile acid.

Authors:  Benny Liu; Charina M Ramirez; Anna M Miller; Joyce J Repa; Stephen D Turley; John M Dietschy
Journal:  J Lipid Res       Date:  2009-11-18       Impact factor: 5.922

5.  Extensive macrophage accumulation in young and old Niemann-Pick C1 model mice involves the alternative, M2, activation pathway and inhibition of macrophage apoptosis.

Authors:  Gail Deutsch; Akshay Muralidhar; Ellen Le; Ivan A Borbon; Robert P Erickson
Journal:  Gene       Date:  2015-12-18       Impact factor: 3.688

6.  Pulmonary abnormalities in animal models due to Niemann-Pick type C1 (NPC1) or C2 (NPC2) disease.

Authors:  Blair R Roszell; Jian-Qin Tao; Kevin J Yu; Ling Gao; Shaohui Huang; Yue Ning; Sheldon I Feinstein; Charles H Vite; Sandra R Bates
Journal:  PLoS One       Date:  2013-07-02       Impact factor: 3.240

  6 in total

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