Literature DB >> 2592300

Isolation of alveolar epithelial cells from lung tissue obtained at autopsy.

D L Shapiro1, J N Finkelstein, T Van Diver.   

Abstract

Lung alveolar epithelial cells have been studied in a variety of laboratory animal models, and studies of human alveolar epithelial cells are important for comparison to information obtained from animal studies. Autopsy material is a source of human cells for study. Studies of human autopsy material revealed variables that negatively affected the yield of viable cells. For specimens from adults, these included death greater than 12 h before cell isolation, obvious severe lung fibrosis, longstanding metabolic disorders, and lung congestion indicated by weight of the right middle lobe greater than 150 g. Samples from children yielded significant numbers of viable cells up to 18 h after death. For 17 specimens that conformed to the above criteria, approximately 8.5 x 10(6) alveolar cells were obtained per gram of tissue (tissue weights ranged from 30 to 108 g) using a procedure involving instillation of proteases into the airways. The cells could be further fractionated, and 10 to 15% of the mixed cells obtained were type II pneumocytes. Analysis of NADPH cytochrome-c-reductase distribution in subcellular fractions provided evidence that the cells obtained were intact. Phospholipid enzyme activities and synthetic activity were within the ranges previously found in laboratory studies of freshly obtained animal lungs. These results suggest that significant numbers of viable and functional human lung cells, including type II pneumocytes, can be obtained from autopsy material.

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Year:  1989        PMID: 2592300     DOI: 10.1007/bf02624140

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  14 in total

1.  A rapid method of total lipid extraction and purification.

Authors:  E G BLIGH; W J DYER
Journal:  Can J Biochem Physiol       Date:  1959-08

2.  Type II epithelial cells from the lung of Syrian hamsters: isolation and metabolism.

Authors:  R C Pfleger
Journal:  Exp Mol Pathol       Date:  1977-10       Impact factor: 3.362

3.  Maintenance of human and rat pulmonary type II cells in an organotypic culture system.

Authors:  W H Douglas; R L Sanders; K R Hitchcock
Journal:  Methods Cell Biol       Date:  1980       Impact factor: 1.441

4.  Immunochemical determination and immunocytological localization of brain-specific protein alpha-albumin (GFA) in isolated astrocytes.

Authors:  J Gheuens; M Noppe; D Karcher; A Lowenthal
Journal:  Neurochem Res       Date:  1980-07       Impact factor: 3.996

5.  Purification and maintenance in culture of oligodendroglia from human multiple sclerosis brain.

Authors:  S E Poduslo; K Miller; S Zoller
Journal:  J Neurol Sci       Date:  1982-06       Impact factor: 3.181

6.  Properties of freshly isolated type II alveolar epithelial cells.

Authors:  J N Finkelstein; W M Maniscalco; D L Shapiro
Journal:  Biochim Biophys Acta       Date:  1983-06-02

7.  Human dihydropteridine reductase: a method for the measurement of activity in cultured cells, and its application to malignant hyperphenylalaninemia.

Authors:  F A Firgaira; R G Cotton; D M Danks
Journal:  Clin Chim Acta       Date:  1979-07-02       Impact factor: 3.786

8.  Effects of ozone on phospholipid synthesis by alveolar type II cells isolated from adult rat lung.

Authors:  H P Haagsman; E A Schuurmans; G M Alink; J J Batenburg; L M van Golde
Journal:  Exp Lung Res       Date:  1985       Impact factor: 2.459

9.  Lamellar bodies isolated from adult human lung tissue.

Authors:  M Post; J J Batenburg; E A Schuurmans; C D Laros; L M van Golde
Journal:  Exp Lung Res       Date:  1982-02       Impact factor: 2.459

10.  Biochemical studies of the late infantile form of metachromatic leukodystrophy.

Authors:  S E Poduslo; K Miller; Y Jang
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

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  2 in total

1.  Monolayers of human alveolar epithelial cells in primary culture for pulmonary absorption and transport studies.

Authors:  K J Elbert; U F Schäfer; H J Schäfers; K J Kim; V H Lee; C M Lehr
Journal:  Pharm Res       Date:  1999-05       Impact factor: 4.200

2.  Cell culture systems and in vitro toxicity testing. Technical report no. 4 of the Johns Hopkins Center for Alternatives to Animal Testing (CAAT): technical workshop of June 13-15, 1990.

Authors: 
Journal:  Cytotechnology       Date:  1992       Impact factor: 2.058

  2 in total

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