» Articles » PMID: 1700614

Neuroendocrine Features of Reactive Bile Ductules in Cholestatic Liver Disease

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 1990 Nov 1
PMID 1700614
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Various cholestatic liver diseases are accompanied by a striking increase in the number of bile ductules. This so-called ductular reaction is thought to arise both from ductular metaplasia of hepatocytes and from proliferation of pre-existing bile ductules. Previous studies have shown that these reactive bile ductules differ from their normal counterpart in enzyme and immunohistochemical make-up. Using monoclonal antibodies directed to neuroendocrine markers and immunohistochemistry, we found that reactive bile ductules in cholestatic liver disease display neuroendocrine features. In all cases of primary biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC), extrahepatic obstruction, and acute hepatitis A, reactive bile ductules expressed the neural cell adhesion molecule (N-CAM) and reacted with monoclonal antibody A2B5. Both N-CAM and the ganglioside, recognized by A2B5, are restricted to neuroendocrine cells and tissues. In all but four of these cases, the same bile ductules expressed chromogranin-A, present in the matrix of neuroendocrine granules. Furthermore, in three cases of longstanding cholestasis, scattered periportal hepatocytes expressed chromogranin-A but not N-CAM. Other neuroendocrine markers such as neuron-specific enolase, synaptophysin, or myelin-associated glycoprotein were lacking from both bile ductules and hepatocytes. The neuroendocrine phenotype of bile ductules and hepatocytes was confirmed on electronmicroscopy, demonstrating various numbers of dense-cored, neuroendocrine granules near the peripheral cell membrane in bile ductules as well as in cells intermediate between hepatocytes and bile ductular cells. In 10 cases of normal liver tissue without ductular reaction, bile ductules lacked neuroendocrine markers except in two cases in which very weak reactivity for chromogranin-A was observed. These findings illustrate the presence of a new, neuroendocrine cell type that emerges in the liver during cholestasis. Elucidation of the significance of the neuroendocrine substance(s) produced in the dense cored granules of reactive bile ductules awaits their isolation and characterization. We can speculate that this molecule plays an autocrine or paracrine regulatory role in the process of ductular metaplasia of hepatocytes or growth of bile ductules.

Citing Articles

Panic at the Bile Duct: How Intrahepatic Cholangiocytes Respond to Stress and Injury.

Hrncir H, Hantelys F, Gracz A Am J Pathol. 2023; 193(10):1440-1454.

PMID: 36870530 PMC: 10548281. DOI: 10.1016/j.ajpath.2023.02.012.


"A Tale of 2 Demons"-Concomitant Presence of Hepatocellular Carcinoma and Primary Neuroendocrine Tumor of Liver: A Case Report and Review of Literatures.

Khanam R, Pachika P, Arya P, Bierenbaum J, Kane K, Saha P J Investig Med High Impact Case Rep. 2021; 9:23247096211043397.

PMID: 34472368 PMC: 8419549. DOI: 10.1177/23247096211043397.


Increased Expression of S100B and RAGE in a Mouse Model of Bile Duct Ligation-induced Liver Fibrosis.

Park J, Kim M, Kim S, Kim H, Jeon Y, Shin H J Korean Med Sci. 2021; 36(14):e90.

PMID: 33847081 PMC: 8042478. DOI: 10.3346/jkms.2021.36.e90.


Incidental Collision Tumor of Hepatocellular Carcinoma and Neuroendocrine Carcinoma.

Yilmaz D, Bayramoglu Z, Unay G, Ayik E, Bassorgun C, Elpek G J Clin Transl Hepatol. 2018; 6(3):339-344.

PMID: 30271748 PMC: 6160311. DOI: 10.14218/JCTH.2017.00076.


Neuroendocrine Neoplasms in Rare Locations: Clinicopathological Features and Review of the Literature.

Diaz Del Arco C, Sastre J, Peinado P, Diaz A, Ortega Medina L, Fernandez Acenero M Indian J Endocrinol Metab. 2018; 22(3):308-315.

PMID: 30090720 PMC: 6063171. DOI: 10.4103/ijem.IJEM_446_17.


References
1.
Lanier L, Testi R, Bindl J, Phillips J . Identity of Leu-19 (CD56) leukocyte differentiation antigen and neural cell adhesion molecule. J Exp Med. 1989; 169(6):2233-8. PMC: 2189344. DOI: 10.1084/jem.169.6.2233. View

2.
Ohtani O . The peribiliary portal system in the rabbit liver. Arch Histol Jpn. 1979; 42(2):153-67. DOI: 10.1679/aohc1950.42.153. View

3.
Wiedenmann B, Huttner W . Synaptophysin and chromogranins/secretogranins--widespread constituents of distinct types of neuroendocrine vesicles and new tools in tumor diagnosis. Virchows Arch B Cell Pathol Incl Mol Pathol. 1989; 58(2):95-121. DOI: 10.1007/BF02890062. View

4.
Simon J, Aunis D . Biochemistry of the chromogranin A protein family. Biochem J. 1989; 262(1):1-13. PMC: 1133222. DOI: 10.1042/bj2620001. View

5.
Langley O, Grant N, Gratzl M . Expression of the neural cell adhesion molecule NCAM in endocrine cells. J Histochem Cytochem. 1989; 37(6):781-91. DOI: 10.1177/37.6.2723399. View