Characterization of choroid plexus in the preterm rabbit pup following subcutaneous administration of recombinant human IGF-1/IGFBP-3

Springer Science and Business Media LLC - Tập 20 - Trang 1-18 - 2023
Niklas Ortenlöf1, Suvi Vallius1, Helena Karlsson2, Claes Ekström2, Amanda Kristiansson2, Bo Holmqvist3, Olga Göransson4, Magdaléna Vaváková4, Martin Rydén5, Galen Carey6, Norman Barton7, David Ley2, Magnus Gram2
1Pediatrics, Department of Clinical Sciences Lund, Lund University, Lund, Sweden
2Pediatrics, Department of Clinical Sciences Lund, Lund University, Skåne University Hospital, Lund, Sweden
3ImaGene-iT AB, Lund, Sweden
4Department of Experimental Medical Science, Lund University, Lund, Sweden
5Orthopaedics, Department of Clinical Sciences Lund, Lund University, Lund, Sweden
6Takeda, Cambridge, USA
7Oak Hill Bio, Scientific Advisory Board, Boston, USA

Tóm tắt

Insulin-like growth factor-1 (IGF-1) is essential for normal brain development and regulates essential processes of vascular maturation and stabilization. Importantly, preterm birth is associated with reduced serum levels of IGF-1 as compared to in utero levels. Using a preterm rabbit pup model, we investigated the uptake of systemic recombinant human (rh) IGF-1 in complex with its main binding protein IGF-binding protein 3 (BP-3) to the brain parenchyma via the choroid plexus. Five hours after subcutaneous administration, labeled rhIGF-1/rhIGFBP-3 displayed a widespread presence in the choroid plexus of the lateral and third ventricle, however, to a less degree in the fourth, as well as in the perivascular and subarachnoid space. We found a time-dependent uptake of IGF-1 in cerebrospinal fluid, decreasing with postnatal age, and a translocation of IGF-1 through the choroid plexus. The impact of systemic rhIGF-1/rhIGFBP-3 on IGF-1 receptor activation in the choroid plexus decreased with postnatal age, correlating with IGF-1 uptake in cerebrospinal fluid. In addition, choroid plexus gene expression was observed to increase with postnatal age. Moreover, using choroid plexus in vitro cell cultures, gene expression and protein synthesis were further investigated upon rhIGF-1/rhIGFBP-3 stimulation as compared to rhIGF-1 alone, and found not to be differently altered. Here, we characterize the uptake of systemic rhIGF-1/rhIGFBP-3 to the preterm brain, and show that the interaction between systemic rhIGF-1/rhIGFBP-3 and choroid plexus varies over time.

Tài liệu tham khảo

Gubbi S, Quipildor GF, Barzilai N, Huffman DM, Milman S. 40 YEARS of IGF1: IGF1: the Jekyll and Hyde of the aging brain. J Mol Endocrinol. 2018;61(1):T171–t85. Fernandez AM, Torres-Aleman I. The many faces of insulin-like peptide signalling in the brain. Nat Rev Neurosci. 2012;13(4):225–39. Gram M, Ekström C, Holmqvist B, Carey G, Wang X, Vallius S, et al. Insulin-like growth factor 1 in the Preterm rabbit pup: characterization of cerebrovascular maturation following administration of recombinant human insulin-like Growth factor 1/Insulin-Like Growth factor 1-Binding protein 3. Dev Neurosci. 2021;43(5):281–95. Hellström A, Ley D, Hansen-Pupp I, Hallberg B, Löfqvist C, van Marter L, et al. Insulin-like growth factor 1 has multisystem effects on foetal and preterm infant development. Acta Paediatr. 2016;105(6):576–86. Hansen-Pupp I, Hövel H, Löfqvist C, Hellström-Westas L, Fellman V, Huppi PS, et al. Circulatory insulin-like growth factor-I and brain volumes in relation to neurodevelopmental outcome in very preterm infants. Pediatr Res. 2013;74(5):564–9. Ley D, Hallberg B, Hansen-Pupp I, Dani C, Ramenghi LA, Marlow N, et al. rhIGF-1/rhIGFBP-3 in Preterm Infants: a phase 2 Randomized Controlled Trial. J Pediatr. 2019;206:56–65e8. Hellstrom A, Ley D, Hallberg B, Lofqvist C, Hansen-Pupp I, Ramenghi LA, et al. IGF-1 as a drug for Preterm Infants: a step-wise Clinical Development. Curr Pharm Des. 2017;23(38):5964–70. Schwartz MW, Sipols A, Kahn SE, Lattemann DF, Taborsky GJ Jr, Bergman RN, et al. Kinetics and specificity of insulin uptake from plasma into cerebrospinal fluid. Am J Physiol. 1990;259(3 Pt 1):E378–83. Carro E, Spuch C, Trejo JL, Antequera D, Torres-Aleman I. Choroid plexus megalin is involved in neuroprotection by serum insulin-like growth factor I. J Neurosci. 2005;25(47):10884–93. van der Merwe J, van der Veeken L, Inversetti A, Galgano A, Toelen J, Deprest J. Earlier preterm birth is associated with a worse neurocognitive outcome in a rabbit model. PLoS ONE. 2021;16(1):e0246008. Romantsik O, Ross-Munro E, Grönlund S, Holmqvist B, Brinte A, Gerdtsson E, et al. Severe intraventricular hemorrhage causes long-lasting structural damage in a preterm rabbit pup model. Pediatr Res. 2022;92(2):403–14. Ferraris S, van der Merwe J, Van Der Veeken L, Prados F, Iglesias JE, Melbourne A, et al. A magnetic resonance multi-atlas for the neonatal rabbit brain. NeuroImage. 2018;179:187–98. Sveinsdóttir S, Cinthio M, Ley D. High-frequency ultrasound in the evaluation of cerebral intraventricular haemorrhage in preterm rabbit pups. Ultrasound Med Biol. 2012;38(3):423–31. Menheniott TR, Charalambous M, Ward A. Derivation of primary choroid plexus epithelial cells from the mouse. Methods Mol Biol. 2010;633:207–20. Laemmli UK. Cleavage of structural proteins during the Assembly of the Head of Bacteriophage T4. Nature. 1970;227(5259):680–5. Willforss J, Chawade A, Levander F. NormalyzerDE: Online Tool for Improved normalization of Omics expression data and high-sensitivity Differential expression analysis. J Proteome Res. 2019;18(2):732–40. Russell V. Lenth. emmeans: Estimated Marginal Means, aka Least-Squares Means. R package version 1.6.1. https://CRAN.R-project.org/package=emmeans; 2021. Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, et al. Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet. 2000;25(1):25–9. Szklarczyk D, Gable AL, Lyon D, Junge A, Wyder S, Huerta-Cepas J, et al. STRING v11: protein-protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets. Nucleic Acids Res. 2019;47(D1):D607–d13. Sherman BT, Hao M, Qiu J, Jiao X, Baseler MW, Lane HC, et al. DAVID: a web server for functional enrichment analysis and functional annotation of gene lists (2021 update). Nucleic Acids Res. 2022;50(W1):W216–W21. Dziegielewska KM, Ek J, Habgood MD, Saunders NR. Development of the choroid plexus. Microsc Res Tech. 2001;52(1):5–20. Richardson SJ, Wijayagunaratne RC, D’Souza DG, Darras VM, Van Herck SL. Transport of thyroid hormones via the choroid plexus into the brain: the roles of transthyretin and thyroid hormone transmembrane transporters. Front Neurosci. 2015;9:66. Johansson PA, Irmler M, Acampora D, Beckers J, Simeone A, Götz M. The transcription factor Otx2 regulates choroid plexus development and function. Development. 2013;140(5):1055–66. Watanabe M, Kang YJ, Davies LM, Meghpara S, Lau K, Chung CY, et al. BMP4 sufficiency to induce choroid plexus epithelial fate from embryonic stem cell-derived neuroepithelial progenitors. J Neurosci. 2012;32(45):15934–45. Hébert JM, Mishina Y, McConnell SK. BMP signaling is required locally to pattern the dorsal telencephalic midline. Neuron. 2002;35(6):1029–41. Fame RM, Lehtinen MK. Emergence and developmental roles of the Cerebrospinal Fluid System. Dev Cell. 2020;52(3):261–75. Liddelow SA. Development of the choroid plexus and blood-CSF barrier. Front NeuroSci. 2015;9. Dani N, Herbst RH, McCabe C, Green GS, Kaiser K, Head JP, et al. A cellular and spatial map of the choroid plexus across brain ventricles and ages. Cell. 2021;184(11):3056–74e21. Saunders NR, Dziegielewska KM, Fame RM, Lehtinen MK, Liddelow SA. The choroid plexus: a missing link in our understanding of brain development and function. Physiol Rev. 2023;103(1):919–56. Kaiser K, Jang A, Kompanikova P, Lun MP, Prochazka J, Machon O et al. MEIS-WNT5A axis regulates development of fourth ventricle choroid plexus. Development. 2021;148(10). Strazielle N, Ghersi-Egea JF. Potential pathways for CNS drug delivery across the blood-cerebrospinal fluid barrier. Curr Pharm Des. 2016;22(35):5463–76. Kompaníková P, Bryja V. Regulation of choroid plexus development and its functions. Cell Mol Life Sci. 2022;79(6):304. Bunn RC, King WD, Winkler MK, Fowlkes JL. Early developmental changes in IGF-I, IGF-II, IGF binding Protein-1, and IGF binding Protein-3 concentration in the Cerebrospinal Fluid of Children. Pediatr Res. 2005;58(1):89–93. Wilson CG, Sarkar PK, Mazumdar J, Bharadhwaj B. Study of glomerular functions in neonates. Med J Armed Forces India. 1999;55(3):183–6. Saunders NR, Dreifuss JJ, Dziegielewska KM, Johansson PA, Habgood MD, Møllgård K, et al. The rights and wrongs of blood-brain barrier permeability studies: a walk through 100 years of history. Front Neurosci. 2014;8:404. Qiu F, Huang Y, Saunders NR, Habgood MD, Dziegielewska KM. Age dependent contribution of entry via the CSF to the overall brain entry of small and large hydrophilic markers. Fluids and Barriers of the CNS. 2022;19(1):90. Carro E, Nunez A, Busiguina S, Torres-Aleman I. Circulating insulin-like growth factor I mediates effects of exercise on the brain. J Neurosci. 2000;20(8):2926–33. Pan WH, Kastin AJ. Interactions of IGF-1 with the blood-brain barrier in vivo and in situ. Neuroendocrinology. 2000;72(3):171–8. Nagaraja TN, Patel P, Gorski M, Gorevic PD, Patlak CS, Fenstermacher JD. In normal rat, intraventricularly administered insulin-like growth factor-1 is rapidly cleared from CSF with limited distribution into brain. Cerebrospinal Fluid Research. 2005;2(1):5. Gordon N. Cerebral folate deficiency. Dev Med Child Neurol. 2009;51(3):180–2. Steinfeld R, Grapp M, Kraetzner R, Dreha-Kulaczewski S, Helms G, Dechent P, et al. Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism. Am J Hum Genet. 2009;85(3):354–63. Larsen KB, Lutterodt MC, Møllgård K, Møller M. Expression of the homeobox genes OTX2 and OTX1 in the early developing human brain. J Histochem Cytochem. 2010;58(7):669–78. Khan S. IGFBP-2 signaling in the brain: from Brain Development to higher Order Brain Functions. Front Endocrinol (Lausanne). 2019;10:822. Pera EM, Wessely O, Li SY, De Robertis EM. Neural and head induction by insulin-like growth factor signals. Dev Cell. 2001;1(5):655–65.