Development of the Pituitary Gland

被引:48
作者
Alatzoglou, Kyriaki S. [1 ]
Gregory, Louise C. [1 ]
Dattani, Mehul, I [1 ]
机构
[1] UCL, UCL Great Ormond St Inst Child Hlth, Genet & Genom Med Programme, London, England
关键词
GROWTH-HORMONE DEFICIENCY; TRANSCRIPTION FACTOR SOX3; SEPTO-OPTIC DYSPLASIA; OF-FUNCTION MUTATIONS; HOMEOBOX GENE HESX1; CELL LINEAGES; STEM-CELLS; STEROIDOGENIC FACTOR-1; STEM/PROGENITOR CELL; SONIC-HEDGEHOG;
D O I
10.1002/cphy.c150043
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The development of the anterior pituitary gland occurs in distinct sequential developmental steps, leading to the formation of a complex organ containing five different cell types secreting six different hormones. During this process, the temporal and spatial expression of a cascade of signaling molecules and transcription factors plays a crucial role in organ commitment, cell proliferation, patterning, and terminal differentiation. The morphogenesis of the gland and the emergence of distinct cell types from a common primordium are governed by complex regulatory networks involving transcription factors and signaling molecules that may be either intrinsic to the developing pituitary or extrinsic, originating from the ventral diencephalon, the oral ectoderm, and the surrounding mesenchyme. Endocrine cells of the pituitary gland are organized into structural and functional networks that contribute to the coordinated response of endocrine cells to stimuli; these cellular networks are formed during embryonic development and are maintained or may be modified in adulthood, contributing to the plasticity of the gland. Abnormalities in any of the steps of pituitary development may lead to congenital hypopituitarism that includes a spectrum of disorders from isolated to combined hormone deficiencies including syndromic disorders such as septo-optic dysplasia. Over the past decade, the acceleration of next-generation sequencing has allowed for rapid analysis of the patient genome to identify novel mutations and novel candidate genes associated with hypothalmo-pituitary development. Subsequent functional analysis using patient fibroblast cells, and the generation of stem cells derived from patient cells, is fast replacing the need for animal models while providing a more physiologically relevant characterization of novel mutations. Furthermore, CRISPR-Cas9 as the method for gene editing is replacing previous laborious and time-consuming gene editing methods that were commonly used, thus yielding knockout cell lines in a fraction of the time. (C) 2020 American Physiological Society.
引用
收藏
页码:389 / 413
页数:25
相关论文
共 249 条
[21]   β-catenin:: A pivot between cell adhesion and Wnt signalling [J].
Bienz, M .
CURRENT BIOLOGY, 2005, 15 (02) :R64-R67
[22]   Distinct Developmental Roles of Cell Cycle Inhibitors p57Kip2 and p27Kip1 Distinguish Pituitary Progenitor Cell Cycle Exit from Cell Cycle Reentry of Differentiated Cells [J].
Bilodeau, Steve ;
Roussel-Gervais, Audrey ;
Drouin, Jacques .
MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (07) :1895-1908
[23]   Molecular Pathways Controlling Development of Thalamus and Hypothalamus: From Neural Specification to Circuit Formation [J].
Blackshaw, Seth ;
Scholpp, Steffen ;
Placzek, Marysia ;
Ingraham, Holly ;
Simerly, Richard ;
Shimogori, Tomomi .
JOURNAL OF NEUROSCIENCE, 2010, 30 (45) :14925-14930
[24]   Revealing the large-scale network organization of growth hormone-secreting cells [J].
Bonnefont, X ;
Lacampagne, A ;
Sanchez-Hormigo, A ;
Fino, E ;
Creff, A ;
Mathieu, MN ;
Smallwood, S ;
Carmignac, D ;
Fontanaud, P ;
Travo, P ;
Alonso, G ;
Courtois-Coutry, N ;
Pincus, SM ;
Robinson, ICAF ;
Mollard, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (46) :16880-16885
[25]   PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency:: A longitudinal analysis [J].
Böttner, A ;
Keller, E ;
Kratzsch, J ;
Stobbe, H ;
Weigel, JFW ;
Keller, A ;
Hirsch, W ;
Kiess, W ;
Blum, WF ;
Pfäffle, RW .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (10) :5256-5265
[26]   Discovery of transcriptional regulators and signaling pathways in the developing pituitary gland by bioinformatic and genomic approaches [J].
Brinkmeier, Michelle L. ;
Davis, Shannon W. ;
Carninci, Piero ;
MacDonald, James W. ;
Kawai, Jun ;
Ghosh, Debashis ;
Hayashizaki, Yoshihide ;
Lyons, Robert H. ;
Camper, Sally A. .
GENOMICS, 2009, 93 (05) :449-460
[27]   TCF4 deficiency expands ventral diencephalon signaling and increases induction of pituitary progenitors [J].
Brinkmeler, Michelle L. ;
Potok, Mary Anne ;
Davis, Shannon W. ;
Camper, Sally A. .
DEVELOPMENTAL BIOLOGY, 2007, 311 (02) :396-407
[28]   The selector gene Pax7 dictates alternate pituitary cell fates through its pioneer action on chromatin remodeling [J].
Budry, Lionel ;
Balsalobre, Aurelio ;
Gauthier, Yves ;
Khetchoumian, Konstantin ;
L'Honore, Aurore ;
Vallette, Sophie ;
Brue, Thierry ;
Figarella-Branger, Dominique ;
Meij, Bjorn ;
Drouin, Jacques .
GENES & DEVELOPMENT, 2012, 26 (20) :2299-2310
[29]   Related pituitary cell lineages develop into interdigitated 3D cell networks [J].
Budry, Lionel ;
Lafont, Chrystel ;
El Yandouzi, Taoufik ;
Chauvet, Norbert ;
Conejero, Genevieve ;
Drouin, Jacques ;
Mollard, Patrice .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (30) :12515-12520
[30]   Vertebrate neurogenesis is counteracted by Sox1-3 activity [J].
Bylund, M ;
Andersson, E ;
Novitch, BG ;
Muhr, J .
NATURE NEUROSCIENCE, 2003, 6 (11) :1162-1168