Unbound (bioavailable) IGF1 enhances somatic growth

Autor: Luis Cardoso, Hui Sun, Jan Frystyk, Hayden William Courtland, Liliana Karabatas, Chengyu Liu, Sebastien Elis, Jelena Basta-Pljakic, Shoshana Yakar, Mordechay Beth-On, Hector Jasper, Yingjie Wu, Clifford J. Rosen, Horacio Domene, Dara Cannata, Clara Guida
Přispěvatelé: Division of Endocrinology, Diabetes and Bone Disease, Icahn School of Medicine at Mount Sinai [New York] (MSSM), National Institutes of Health, Ricardo Gutierrez Children's Hospital, Partenaires INRAE, City College of New York, Maine Medical Center Research Institute (MMCRI), Aarhus University [Aarhus], NIH, United States AR054919 AR055141, NIH/NIA, United States AG034198, NIH/HLI, United States HL101157, NSF/MRI, United States CBET-0723027, NIH/NIAMS, United States AR53853 AR45433, Argentina CONICET PIP 11420090100045
Jazyk: angličtina
Rok vydání: 2011
Předmět:
Somatic cell
Mutant
Uterus
Medicine (miscellaneous)
Ciencias de la Salud
lcsh:Medicine
Plasma protein binding
souris
Mice
0302 clinical medicine
Immunology and Microbiology (miscellaneous)
IGF1 bioactivity
Osteogenesis
développement corporel
knock-in mouse models of mutated IGF1
Body Size
Gene Knock-In Techniques
Insulin-Like Growth Factor I
Peptide sequence
Ternary complex
0303 health sciences
Organ Size
3. Good health
Otras Ciencias de la Salud
medicine.anatomical_structure
030220 oncology & carcinogenesis
Models
Animal

purl.org/becyt/ford/3 [https]
Female
Growth and Development
hormones
hormone substitutes
and hormone antagonists

lcsh:RB1-214
Autre (Sciences du Vivant)
Research Article
Protein Binding
medicine.medical_specialty
[SDV.OT]Life Sciences [q-bio]/Other [q-bio.OT]
endocrine system
CIENCIAS MÉDICAS Y DE LA SALUD
education
Molecular Sequence Data
Neuroscience (miscellaneous)
Biological Availability
030209 endocrinology & metabolism
Spleen
Biology
General Biochemistry
Genetics and Molecular Biology

03 medical and health sciences
purl.org/becyt/ford/3.3 [https]
Immune system
Mammary Glands
Animal

Internal medicine
medicine
lcsh:Pathology
Animals
Amino Acid Sequence
Gene
030304 developmental biology
Base Sequence
lcsh:R
Body Weight
Wild type
Cell Biology
facteur de croissance igf 1
Mice
Mutant Strains

Mice
Inbred C57BL

Endocrinology
insulin-like growth factor-1 (IGF1)
Growth Hormone
Multiprotein Complexes
Zdroj: Elis, S, Wu, Y, Courtland, H-W, Cannata, D, Sun, H, Beth-On, M, Liu, C, Jasper, H, Domené, H, Karabatas, L, Guida, C, Basta-Pljakic, J, Cardoso, L, Rosen, C J, Frystyk, J & Yakar, S 2011, ' Unbound (bioavailable) IGF1 enhances somatic growth ', Disease Models and Mechanisms, vol. 4, no. 5, pp. 649-58 . https://doi.org/10.1242/dmm.006775
Disease Models & Mechanisms
Disease Models & Mechanisms, Cambridge Company of Biologists, 2011, 4 (5), pp.649-658. ⟨10.1242/dmm.006775⟩
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Disease Models and Mechanisms 5 (4), 649-658. (2011)
Disease Models & Mechanisms, Vol 4, Iss 5, Pp 649-658 (2011)
ISSN: 1754-8403
1754-8411
DOI: 10.1242/dmm.006775
Popis: Understanding insulin-like growth factor-1 (IGF1) biology is of particular importance because, apart from its role in mediating growth, it plays key roles in cellular transformation, organ regeneration, immune function, development of the musculoskeletal system and aging. IGF1 bioactivity is modulated by its binding to IGF-binding proteins (IGFBPs) and the acid labile subunit (ALS), which are present in serum and tissues. To determine whether IGF1 binding to IGFBPs is necessary to facilitate normal growth and development, we used a gene-targeting approach and generated two novel knock-in mouse models of mutated IGF1, in which the native Igf1 gene was replaced by Des-Igf1 (KID mice) or R3-Igf1 (KIR mice). The KID and KIR mutant proteins have reduced affinity for the IGFBPs, and therefore present as unbound IGF1, or ‘free IGF1’. We found that both KID and KIR mice have reduced serum IGF1 levels and a concomitant increase in serum growth hormone levels. Ternary complex formation of IGF1 with the IGFBPs and the ALS was markedly reduced in sera from KID and KIR mice compared with wild type. Both mutant mice showed increased body weight, body and bone lengths, and relative lean mass. We found selective organomegaly of the spleen, kidneys and uterus, enhanced mammary gland complexity, and increased skeletal acquisition. The KID and KIR models show unequivocally that IGF1-complex formation with the IGFBPs is fundamental for establishing normal body and organ size, and that uncontrolled IGF bioactivity could lead to pathological conditions. Fil: Elis, Sebastien. Mount Sinai School of Medicine; Estados Unidos Fil: Wu, Yingjie. Mount Sinai School of Medicine; Estados Unidos Fil: Courtland, Hayden William. Mount Sinai School of Medicine; Estados Unidos Fil: Cannata, Dara. Mount Sinai School of Medicine; Estados Unidos Fil: Sun, Hui. Mount Sinai School of Medicine; Estados Unidos Fil: Beth On, Mordechay. Mount Sinai School of Medicine; Estados Unidos Fil: Liu, Chengyu. National Institutes of Health; Estados Unidos Fil: Jasper, Hector Guillermo. Gobierno de la Ciudad Autonoma de Buenos Aires. Hospital General de Niños "ricardo Gutierrez". Departamento de Medicina.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Domené, Horacio. Gobierno de la Ciudad Autonoma de Buenos Aires. Hospital General de Niños "ricardo Gutierrez". Departamento de Medicina.; Argentina Fil: Karabatas, Liliana Margarita. Gobierno de la Ciudad Autonoma de Buenos Aires. Hospital General de Niños "ricardo Gutierrez". Departamento de Medicina.; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Guida, Clara. Gobierno de la Ciudad Autonoma de Buenos Aires. Hospital General de Niños "ricardo Gutierrez". Departamento de Medicina.; Argentina Fil: Basta Pljakic, Jelena. City University Of New York. The City College Of New York.; Estados Unidos Fil: Cardoso, Luis. City University Of New York. The City College Of New York.; Estados Unidos Fil: Rosen, Clifford J.. Maine Medical Center Research Institute; Estados Unidos Fil: Frystyk, Jan. Aarhus University Hospital; Dinamarca Fil: Yakar, Shoshana. Mount Sinai School of Medicine; Estados Unidos
Databáze: OpenAIRE