Literature DB >> 17976156

Lack of cilia and differentiation defects in the liver of human foetuses with the Meckel syndrome.

Frédéric Clotman1, Louis Libbrecht, Murray C Killingsworth, Christine C K Loo, Tania Roskams, Frédéric P Lemaigre.   

Abstract

BACKGROUND/AIMS: Meckel syndrome is an autosomal-recessive disease characterized by a combination of renal cysts, anomalies of the central nervous system, polydactyly and ductal plate malformations (DPM), which are hepatic anomalies consisting of excessive and abnormal foetal biliary structures. Among the genomic loci associated with Meckel syndrome, mutations in four genes were recently identified. These genes code for proteins associated with primary cilia and are possibly involved in cell differentiation. The aim of the present work was to investigate the formation of the primary cilia and the differentiation of the hepatic cells in foetuses with Meckel syndrome.
METHODS: Sections of livers from human foetuses with Meckel syndrome were analysed by immunofluorescence, immunohistochemistry and electron microscopy.
RESULTS: The primary cilia of the biliary cells were absent in some Meckel foetuses, but were present in others. In addition, defects in hepatic differentiation were observed in Meckel livers, as evidenced by the presence of hybrid cells co-expressing hepatocytic and biliary markers.
CONCLUSIONS: Defects in cilia formation occur in some Meckel livers, and most cases show DPM associated with abnormal hepatic cell differentiation. Because differentiation precedes the formation of the cilia during liver development, we propose that defective differentiation may constitute the initial defect in the liver of Meckel syndrome foetuses.

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Year:  2007        PMID: 17976156     DOI: 10.1111/j.1478-3231.2007.01617.x

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  8 in total

1.  Loss of Anks6 leads to YAP deficiency and liver abnormalities.

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2.  Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3.

Authors:  Rachaneekorn Tammachote; Cynthia J Hommerding; Rachel M Sinders; Caroline A Miller; Peter G Czarnecki; Amanda C Leightner; Jeffrey L Salisbury; Christopher J Ward; Vicente E Torres; Vincent H Gattone; Peter C Harris
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3.  Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle.

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Review 4.  The primary cilium in different tissues-lessons from patients and animal models.

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5.  Embryonic and foetal expression patterns of the ciliopathy gene CEP164.

Authors:  L A Devlin; S A Ramsbottom; L M Overman; S N Lisgo; G Clowry; E Molinari; L Powell; C G Miles; J A Sayer
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6.  Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.

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7.  Immunohistochemical detection of polyductin and co-localization with liver progenitor cell markers during normal and abnormal development of the intrahepatic biliary system and in adult hepatobiliary carcinomas.

Authors:  Livia Dorn; Luís F Menezes; Gregor Mikuz; Herwart F Otto; Luiz F Onuchic; Consolato Sergi
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8.  Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant.

Authors:  Megan G Davey; Lynn McTeir; Andrew M Barrie; Lucy J Freem; Louise A Stephen
Journal:  Organogenesis       Date:  2014-04-17       Impact factor: 2.500

  8 in total

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