Histopathology of α1–Antitrypsin Liver Disease in A... : Hepatology (original) (raw)

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Histopathology of α1–Antitrypsin Liver Disease in A Transgenic Mouse Model

Geller, Stephen A.*,1; Nichols, Stephen W.1; Dycaico, Mark J.2; Felts, Katherine A.2; Sorge, Joseph A.2

1_Department of Pathology and Laboratory Medicine, Cedars–Sinai Medical Center, Los Angeles, California 90048_

2_Stratagene, La Jolla, California 92037_

* Department of Pathology and Laboratory Medicine, Cedars–Sinai Medical Center, 8700 Beverly Boulevard, Los Angeles, CA 90048.

Received: 19 June 1989; Accepted: 20 February 1990

Abstract

Transgenic mice were constructed using human α1–antitrypsin M and Z genomic clones. Livers of the M lineage mice showed slight cellular pleomorphism and immunohistochemically demonstrable finely granular α1–antitrypsin material in hepatocytes. Z lineage mice with five gene copies per haploid mouse genome (Z # 1) demonstrated fine granular α1–antitrypsin material and a few large globules. In contrast, Z lineage mice with 12 gene copies per haploid mouse genome (Z # 2) demonstrated hepatocytes filled with homogeneous, eosinophilic globules that were strongly reactive with diastase and periodic acid-Schiff and antibody to α1–antitrypsin. Scattered microscopic polymorphonuclear leukocyte accumulations were seen that contained extracellular α1–antitrypsin material, but there was neither histological nor serological evidence of mouse infectious hepatitis. In young animals, small clusters of hepatocytes lacking α1–antitrypsin material were seen. These cells were the dominant population in older animals and formed nodular arrangements. Fibrosis was not demonstrable in neonatal and young animals or in any of the controls, but perisinusoidal fibrosis was seen in older Z # 2 mice. Groups of hepatocytes without α1–antitrypsin material showed dysplastic changes. We conclude that the transgenic mouse is a reliable and useful model in which to study the effects of α1–antitrypsin in the liver because it demonstrates changes similar to those in the human disease. (Hepatology 1990;12:40-47).