HIP/PAP gene, encoding a C-type lectin overexpressed in primary liver cancer, is expressed in nervous system as well as in intestine and pancreas of the postimplantation mouse embryo

Citation
C. Lasserre et al., HIP/PAP gene, encoding a C-type lectin overexpressed in primary liver cancer, is expressed in nervous system as well as in intestine and pancreas of the postimplantation mouse embryo, AM J PATH, 154(5), 1999, pp. 1601-1610
Citations number
39
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
AMERICAN JOURNAL OF PATHOLOGY
ISSN journal
00029440 → ACNP
Volume
154
Issue
5
Year of publication
1999
Pages
1601 - 1610
Database
ISI
SICI code
0002-9440(199905)154:5<1601:HGEACL>2.0.ZU;2-0
Abstract
We originally isolated the HIP/PAP gene in a differential screen of a human hepatocellular carcinoma cDNA Library. This gene is expressed at high leve ls in 25% of primary liver cancers but not in nontumorous liver. HIP/PAP be longs to the family of C-type lectins and acts as an adhesion molecule for hepatocytes. In normal adult human tissues, HIP/PAP expression is found in pancreas (exocrine and endocrine cells) and small intestine (Paneth and neu roendocrine cells). In order to gain insight into the possible role of HIP/ PAP in vivo, we have investigated the pattern of HIP/PAP expression in the developing postimplantation mouse embryo by in situ hybridization. Detailed analysis of developing mouse embryos revealed that HIP/PAP gene exhibits a restricted expression pattern during development. Thus, HIP/PAP transcript s are first observed within the nervous system from day 14.5 onwards in tri geminal ganglia, dorsal root ganglia, and spinal cord where it appears to b e an early specific marker of a subpopulation of motor neurons. At laster s tages, HIP/PAP transcripts were detected in intestine and pancreas at day 1 6.5 but not in embryonic liver. This highly restricted expression pattern s uggests that HIP/PAP might participate in neuronal as well as intestinal an d pancreatic cell development.