An Animal Model of Pediatric Combined Pituitary Hormone Deficiency Disease.

2010 ◽  
pp. P3-694-P3-694
Author(s):  
SC Colvin ◽  
RE Malik ◽  
AD Showalter ◽  
KW Sloop ◽  
SJ Rhodes
Endocrinology ◽  
2013 ◽  
Vol 154 (2) ◽  
pp. 738-748 ◽  
Author(s):  
Kelly L. Prince ◽  
Stephanie C. Colvin ◽  
Soyoung Park ◽  
Xianyin Lai ◽  
Frank A. Witzmann ◽  
...  

Combined pituitary hormone deficiency (CPHD) diseases result in severe outcomes for patients including short stature, developmental delays, and reproductive deficiencies. Little is known about their etiology, especially the developmental profiles and the influences of genetic background on disease progression. Animal models for CPHD provide valuable tools to investigate disease mechanisms and inform diagnostic and treatment protocols. Here we examined hormone production during pituitary development and the influence of genetic background on phenotypic severity in the Lhx3W227ter/W227ter mouse model. Lhx3W227ter/W227ter embryos have deficiencies of ACTH, α-glycoprotein subunit, GH, PRL, TSHβ, and LHβ during prenatal development. Furthermore, mutant mice have significant reduction in the critical pituitary transcriptional activator-1 (PIT1). Through breeding, the Lhx3W227ter/W227ter genotype was placed onto the 129/Sv and C57BL/6 backgrounds. Intriguingly, the genetic background significantly affected viability: whereas Lhx3W227ter/W227ter animals were found in the expected frequencies in C57BL/6, homozygous animals were not viable in the 129/Sv genetic environment. The hormone marker and PIT1 reductions observed in Lhx3W227ter/W227ter mice on a mixed background were also seen in the separate strains but in some cases were more severe in 129/Sv. To further characterize the molecular changes in diseased mice, we conducted a quantitative proteomic analysis of pituitary proteins. This showed significantly lower levels of PRL, pro-opiomelanocortin (ACTH), and α-glycoprotein subunit proteins in Lhx3W227ter/W227ter mice. Together, these data show that hormone deficiency disease is apparent in early prenatal stages in this CPHD model system. Furthermore, as is noted in human disease, genetic background significantly impacts the phenotypic outcome of these monogenic endocrine diseases.


Author(s):  
Damian Rogoziński ◽  
Aleksandra Gilis-Januszewska ◽  
Łukasz Kluczyński ◽  
Magdalena Godlewska ◽  
Alicja Hubalewska-Dydejczyk

2016 ◽  
Vol 174 (6) ◽  
pp. R239-R247 ◽  
Author(s):  
Frederic Castinetti ◽  
Rachel Reynaud ◽  
Alexandru Saveanu ◽  
Nicolas Jullien ◽  
Marie Helene Quentien ◽  
...  

Over the last 5 years, new actors involved in the pathogenesis of combined pituitary hormone deficiency in humans have been reported: they included a member of the immunoglobulin superfamily glycoprotein and ciliary G protein-coupled receptors, as well as new transcription factors and signalling molecules. New modes of inheritance for alterations of genes encoding transcription factors have also been described. Finally, actors known to be involved in a very specific phenotype (hypogonadotroph hypogonadism for instance) have been identified in a wider range of phenotypes. These data thus suggest that new mechanisms could explain the low rate of aetiological identification in this heterogeneous group of diseases. Taking into account the fact that several reviews have been published in recent years on classical aetiologies of CPHD such as mutations ofPOU1F1orPROP1, we focused the present overview on the data published in the last 5 years, to provide the reader with an updated review on this rapidly evolving field of knowledge.


2017 ◽  
Vol 62 (8) ◽  
pp. 755-762 ◽  
Author(s):  
Eleonore Bertko ◽  
Jürgen Klammt ◽  
Petra Dusatkova ◽  
Mithat Bahceci ◽  
Nazli Gonc ◽  
...  

10.1038/76041 ◽  
2000 ◽  
Vol 25 (2) ◽  
pp. 182-186 ◽  
Author(s):  
Irène Netchine ◽  
Marie-Laure Sobrier ◽  
Heiko Krude ◽  
Dirk Schnabel ◽  
Mohamed Maghnie ◽  
...  

2011 ◽  
pp. P1-266-P1-266
Author(s):  
Debora Cristina Moraes ◽  
Karina Schiavoni Scandelai Cardoso dos Reis ◽  
Gisele Dazzi Lorenzoni ◽  
Flavia Lucia Conceicao ◽  
Mario Vaismann ◽  
...  

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