Drug Res (Stuttg) 2018; 68(01): 5-16
DOI: 10.1055/s-0043-113637
Review
© Georg Thieme Verlag KG Stuttgart · New York

Action Plan for Prolongation of Nephrogenesis in Preterm and Growth Restricted Babies: Explore Ultrastructure of the Nephrogenic Zone, Identify a Molecular Target, Select a Viable Drug and Find a Path for Administration

Will W. Minuth
1   Institute of Anatomy, University of Regensburg, Regensburg, Germany
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received 04. Mai 2017

accepted 12. Juni 2017

Publikationsdatum:
12. Juli 2017 (online)

Abstract

A large amount of investigations informs about primary steps of mammalian kidney development such as anlage of the organ and initial nephron formation, while only few data exists about the late phase of human kidney development. In particular, little attention was up to date addressed to the decrease of morphogenic activity in the nephrogenic zone short before birth and the vanishing of all stem cell niches aligned beyond the organ capsule. There is evidence that molecular controlling of this normal but degenerative developmental process also plays a decisive role in the kidneys of preterm and growth restricted babies. Although they are born in a phase of active nephrogenesis, a substantial percentage of them evolves oligonephropathy, formation of atypical glomeruli and immaturity of parenchyma. Pathologic findings point out that independent from chemical nature all suspected hampering influences sublimate in the nephrogenic zone. However, it is unknown, whether impaired nephrogenesis is locally caused by harming interstitial fluid, disturbance of morphogen signaling, unbalanced synthesis of extracellular matrix or limited cell to cell communication. Thus, first of all these issues must be resolved, then save application of medicines prolonging nephrogenesis waits for realization. Due to the unexpectedly complex microanatomy and physiology of the nephrogenic zone, it will be a particular challenge for the future.

 
  • References

  • 1 Reidy KJ, Rosenblum ND. Cell and molecular biology of kidney development. Semin Nephrol. 2009; 29: 321-337
  • 2 Nagalakshmi VK, Yu J. The ureteric bud epithlium: Morphogenesis and roles in metanephric kidney patterning. Mol Reprod Dev. 2015; 82: 151-166
  • 3 Faa G, Sanna A, Gerosa C. et al. Renal physiological regenerative medicine to prevent chronic renal failure: Should we start at birth?. Clin Chim Acta 2015; 444: 156-162
  • 4 Abitbol CL, De Freitas MJ, Strauss J. Assessment of kidney function in preterm infants: Lifelong implications. Pediatr. Nephrol. 2016; 31: 2213-2222
  • 5 Luyckx VA, Perico N, Somaschini M. et al. A developmental approach to the prevention of hypertension and kidney disease: A report from the low birth weight and nephron number working group. Lancet 2017; pii: S0140-6736(17)30576-7 DOI: 10.1016/S0140-6736(17)30576-7.
  • 6 Kandasamy Y, Smith R, Wright IM. et al. Extra-uterine growth in preterm infants: Oligonephropathy and prematurity. Pediatr Nephrol 2013; 28: 1791-1796
  • 7 Stritzke A, Thomas S, Amin H. et al. Renal consequences of preterm birth. Molecular and Cellular Pediatrics 2017; 4: 2
  • 8 Sanna A, Fanos V, Gerosa C. et al. Immunohistochemical markers of stem/progenitor cells in the developing human kidney. Acta Histochem. 2015; 117: 437-443
  • 9 Noto A, Fanos V, Dessi A. Metabolomics in newborns. Adv Clin Chem 2016; 74: 35-61
  • 10 Fanni D, Gerosa C, Nemolato S. et al. “Physiological” renal regenerating medicine in VLBW preterm infants: Could a dream come true?. J Matern Fetal Neonatal Med 2012; 25: 41-48
  • 11 Fanos V. Castagnola Faa G. Prolonging nephrogenesis in preterm infant: a new approach for prevention of kidney disease in adulthood. Iran J Kidney Dis 2015; 9: 180-185
  • 12 Saboktakin MR, Tabatabaei RM. Supramolecular hydrogels as drug delivery systems. Int J Biol Macromol. 2015; 75: 426-436
  • 13 Curtis LM, Chen S, Chen B. et al. Contribution of intrarenal cells to cellular repair after acute kidney injury: Subcapsular implantation technique. Am J Physiol Renal Physiol 2008; 295: F310-F314
  • 14 Rumballe BA, Georgas KM, Combes AN. et al. Nephron formation adopts a novel spatial topology at cessation of nephrogenesis. Dev Biol. 2011; 360: 110-122
  • 15 Fanni D, Sanna A, Gerosa C. et al. Each niche has an actor: Multiple stem cell niches in the preterm kidney. Ital J Pediatr 2015; 41: 78
  • 16 Minuth WW, Denk L. Structural links between the renal stem/progenitor cell niche and the organ capsule. Histochem Cell Biol 2014; 141: 459-471
  • 17 Kloth S, Aigner J, Brandt E. et al. Histochemical markers reveal an unexpected heterogeneous composition of the renal embryonic collecting duct epithelium. Kidney Int. 1993; 44: 527-536
  • 18 Park HC, Yasuda K, Kuo MC. et al. Renal capsule as a stem cell niche. Am J Physiol Renal Physiol 2010; 298: F1254-F1262
  • 19 Fanni D, Gerosa C, Vinci L. et al. Interstitial stromal progenitors during kidney development: Here, there and everywhere. J Matern Fetal Neonatal Med 2016; 29: 3815-3820
  • 20 Al-Awqati Q, Goldberg MR. Architectural patterns in branching morphognesis in the kidney. Kidney Int. 1998; 54: 1832-1842
  • 21 Minuth WW. View onto the nephrogenic zone before stem cell niches come apart: Challenge for smart drug delivery. J Drug Res Dev 2017; 3:http://dx.doi.org/10.16966/2470-1009.127
  • 22 Combes AN, Davies JA, Little MH. Cell-cell interactions driving kidney morphogenesis. Curr Top Dev Biol. 2015; 112: 467-508
  • 23 Minuth WW, Denk L, Miess C. et al. Peculiarities of the extracellular matrix in the interstitium of the renal stem/progenitor cell niche. Histochem Cell Biol 2011; 136: 321-334
  • 24 Minuth WW, Denk L. Illustration of extensive extracellular matrix at the epithelial-mesenchymal interface within the renal stem/progenitor cell niche. BMC Clin Pathol 2012; 12: 16
  • 25 Schumacher K, Strehl R, de Vries U. et al. SBA-positive fibers between the CD ampulla, mesenchyme and renal capsule. J Am Soc Nephrol. 2002; 13: 2446-2453
  • 26 Schumacher K, Strehl R, Minuth WW. Characterization of Micro-fibers at the interface between the renal collecting duct ampulla and the cap condensate. Nephron Exp Nephrol. 2003; 95: e43-e54
  • 27 Ikeya M, Fukushima K, Kawada M. et al. Cv2, functioning as a pro-BMP factor via twisted gastrulation, is required for early development of nephron precursors. Development 2010; 337: 405-414
  • 28 Minuth WW, Denk L. The interstitial interface within the renal stem/progenitor cell niche exhibits an unique microheterogenous composition. Int J Mol Sci. 2013; 14: 13657-13569
  • 29 Qiao J, Cohen D, Herzlinger D. The metanephric blastema differentiates into collecting duct system and nephron epithelia in vitro. Development 1995; 121: 3207-3214
  • 30 Kanwar YS, Zheng ZL, Kumar A. et al. D-glucose-induced dysmorphogenesis of embryonic kidney. J Clin Invest. 1996; 98: 2478-2488
  • 31 Barasch J, Yang J, Qiao J. et al. Tissue inhibitor of metalloproteinase-2 stimulates mesenchymal growth and regulates epithelial branching during morphogenesis of the rat metanephros. J Clin Invest. 1999; 103: 1299-1207
  • 32 Strehl R, Trautner V, Kloth S. et al. Existence of a dense reticular meshwork surrounding the nephron inducer in neonatal rabbit kidney. Cell Tissue Res. 1999; 298: 539-548
  • 33 Strehl R, Minuth WW. Partial identification of the mab (CD)Amp1 antigen at the epithelial-mesenchymal interface in the developing kidney. Histochem Cell Biol 2001; 116: 389-396
  • 34 Minuth WW, Denk L. Advanced fixation for transmission electron microscopy unveils special extracellular matrix within the renal stem/progenitor cell niche. Methods Mol Biol. 2015; 1212: 21-23
  • 35 Minuth WW, Denk L. Cell projections and extracellular matrix cross the interstitial interface within the renal stem/progenitor cell niche: Accidental, structural or functional cues?. Nephron Exp Nephrol 2012; 122: 131-140
  • 36 Schumacher K, Klar J, Wagner C. et al. Temporal-spatial co-localisation of tissue transglutaminase (Tgase2) and matrix metalloproteinase-9 (MMP-9) with SBA-positive micro-fibers in the embryonic kidney cortex. Cell Tissue Res. 2005; 319: 491-500
  • 37 Riggins KS, Mernaugh G, Su Y. et al. MT1-MMP-mediated basement membrane remodeling modules renal development. Exp Cell Res. 2010; 316: 2993-3005
  • 38 Zhang Z, Xing J, Gong R. et al. Transglutaminase-1 regulates renal epithelial cell proliferation through activation of Stat-3. J Biol Chem. 2009; 284: 3345-3353
  • 39 Antonyak MA, Li B, Regan AD. et al. Tissue transglutaminase is an essential participant in the epidermal growth factor-stimulated signaling pathway leading to cancer cell migration and invasion. J Biol Chem. 2009; 284: 17914-17925
  • 40 Keillor JW, Apperley KY. Transglutaminase inhibitors: A patent review. Expert Opin Ther Pat 2016; 24: 49-63
  • 41 Müller U, Wang D, Denda S. et al. Integrin α8β1 is critically important for epithelial-mesenchymal interactions during kidney morphogenesis. Cell 1997; 88: 603-613
  • 42 Brandenberger R, Schmidt A, Linton J. et al. Identification and characterization of a novel extracellular matrix protein nephronection that is associated with integrin α8β1 in the embryonic kidney. J Cell Biol. 2001; 154: 447-458
  • 43 Sato Y, Shimono C, Li S. et al. Nephronectin binds to heparan sulfate proteoglycans via MAM domain. Matrix Biol. 2013; 32: 188-195
  • 44 Uchiyama Y, Sakaguchi M, Terebayashi T. et al. Kif26b, a kinesin family gene, regulates adhesion of the embryonic kidney mesenchyme. Proc Natl Acad Sci USA 2010; 107: 9240-9245
  • 45 Nishinakamura R, Uchiyama Y, Sakaguchi M. et al. Nephron progenitors in the metanephric mesenchyme. Pediatr Nephrol. 2011; 26: 1463-1467
  • 46 Minuth WW, Denk L. When morphogenetic proteins encounter special extracellular matrix and cell-cell connections at the interface of the renal stem/progenitor cell niche. Anatomy Cell Biology 2015; 48: 1-9
  • 47 Domhan S, Ma L, Tai A. et al. Intercellular communication by exchange of cytoplasmic material vis tunneling nano-tube like structures in primary human renal epithelial cells. PLoS One 2011; 6: e21283
  • 48 Krause M, Rak-Raszewska A, Pietilä I. et al. Signaling during kidney development. Cells 2015; 4: 112-132
  • 49 Hilliard SA, Yao X, El-Dahr SS. Mdm2 is required for maintenance of the nephrogenic niche. Dev Biol. 2014; 387: 1-14
  • 50 Kobayashi A, Valerius MT, Mugford JW. et al. Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development. Cell Stem Cell 2008; 3: 169-181
  • 51 Kopan R, Chen S, Little M. Nephron progenitor cells: Shifting the balance of self-renewal and differentiation. Curr Top Dev Biol. 2014; 107: 293-331
  • 52 Carroll TJ, Das A. Defining the signals that constitute the nephron progenitor niche. J Am Soc Nephrol. 2013; 24: 873-876
  • 53 Michos O, Goncalves A, Lopez-Rios J. et al. Reduction of BMP4 activity by gremlin 1 enables ureteric bud outgrowth and GNDF/Wnt11 feedback signaling during kidney branching morphogenesis. Development 2007; 134: 2397-2405
  • 54 Faa G, Gerosa C, Fanni D. et al. Morphogenesis and molecular mechanisms involved in human kidney development. J Cell Physiol. 2012; 227: 1257-1268
  • 55 Chai OH, Song CH, Park SK. et al. Molecular regulation of kidney development. Anat Cell Biol 2013; 46: 19-31
  • 56 O’Brien LL, Mc Mahon AP. Induction and patterning of the metanephric nephron. Semin Cell Dev Biol. 2014; 36: 31-38
  • 57 Oxburgh L, Brown AC, Muthukrishnan SD. et al. Bone morphogenetic protein signaling in nephron progenitor cells. Pediatr Nephrol. 2014; 29: 531-536
  • 58 Brazil DP, Church RH, Surae S. et al BMP signalling: Agony and antogony in the family. Trends Cell Biol. 2015; 25: 249-264
  • 59 Piludu M, Fanos V, Congiu T. et al. The pine-cone body: An intermediate structure between the cap mesenchyme and the renal vesicle in the developing nof mouse kidney revealed by an ultrastructural study. J Matern Fetal Neonatal Med 2012; 25: 72-75
  • 60 Potter SS, Brunskill EW, Patterson LT. defining the genetic blueprint of kidney development. Pediatr Nephrol. 2011; 26: 1469-1478
  • 61 Kispert A, Vainio S, McMahon AP. Wnt-4 is a mesenchymal signal for epithelial transformation of metanephric mesenchyme in the developing kidney. Development 1998; 125: 4225-4234
  • 62 Rak-Raszewska A, Hauser PV, Vainio S. Organ in vitro culture: what have we learned about early kidney development. Stem Cells Int 2015; 959807
  • 63 Lehtonen E. Epithelio-mesenchymal interface during mouse kidney tubule induction in vivo. J Embryol Exp Morph 1975; 34: 695-705
  • 64 Saxen L, Lehtonen E. Transfilter induction of kidney tubules as a function of the extent and duration of intercellular contacts. J Embryol Exp Morphol 1978; 47: 97-109
  • 65 Migliorini E, Thakar D, Kühnle J et al. Cytokines and growth factors cross-link heparin sulfate. Open Biol. 2015; 5: pii: 150046
  • 66 Fairchild CL, Barna M. Specialized filopodia: At the ‘tip’ of morphogen transport and vertebrate tissue patterning. Curr Opin Genet Dev 2014; 27: 67-73
  • 67 Lander AD. Morpheus unbound: Reimagining the morphogen gradient. Cell 2007; 128: 245-256
  • 68 Abuharbeid S, Czubayko F, Aigner A. The fibroblast growth factor-binding protein FGF-BP. Int J Biochem Cell Biol. 2006; 38: 1463-1468
  • 69 Swencki-Underwood B, Mills JK, Vennarini J. et al. Expression and characterization of a human BMP-7 variant with improved biochemical properties. Protein Expr Purif. 2008; 57: 312-319
  • 70 Pohl TL, Boergemann JH, Schwaerzer GK. et al. Surface immobilization of bone morphogenetic protein 2 via self-assembled monolayer formation induces cell differentiation. Acta Biomater. 2012; 8: 772-780
  • 71 Creanga A, Glenn TD, Mann RK. et al. Scube/You activity mediates release of dually lipid-modified Hedgehog signal in soluble form. Genes Dev. 2012; 26: 1312-1325
  • 72 Gross JC, Boutros M. Secretion and extracellular space travel of Wnt proteins. Curr Opin Genet Dev 2013; 23: 385-390
  • 73 Bandari S, Exner S, Ortmann C. et al. Sweet on Hedgehogs: regulatory roles of heparin sulfate proteoglycans in Hedgehog-dependent cell proliferation and differentiation. Curr Protein Pept Sci. 2015; 16: 66-76
  • 74 Minuth WW, Denk L. What is the functional background of filigree extracellular matrix and cell-cell connections at the interface of the renal stem/progenitor cell niche?. J Pediatric Neonatal Individualized Medicine 2016; 5: e50115
  • 75 Minuth WW, Denk L. Special morphological features at the interface of the renal stem/progenitor cell niche force to reinvestigate transport of morphogens during nephron induction. BioResearch Open Access 2016; 5: 49-60
  • 76 Akiyama T, Gibson MC. Morphogen transport: Theoretical and experimental controversies. Wiley Interdiscip Rev Dev Biol 2015; 4: 99-112
  • 77 Gheisari Y, Yokko T, Matsumoto K. et al. A thermoreversible polymer mediates controlled release of glial cell line-derived neurotrophic factor to enhance kidney regeneration. Artif Organs. 2010; 34: 642-647
  • 78 Costantini F, Kopan R. Patterning a complex organ: Branching morphogenesis and nephron segmentation in kidney development. Dev Cell. 2010; 18: 698-712
  • 79 Yan D, Lin X. Shaping morphogen gradients by proteoglycans. Cold Spring Harb Perspect Biol 2009; 1: a002493
  • 80 Rosines E, Schmidt HJ, Nigam SK. The effect of hyaluronic acid size and concentration on branching morphogenesis and tubule differentiation in developing kidney culture systems: Potential applications to engineering of renal tissues. Biomaterials 2007; 28: 4806-4817
  • 81 Shah M, Sakurai H, Sweeney DE. et al. Hs2st mediated kidney kidney mesenchyme induction regulates early ureteric bud branching. Dev Biol. 2010; 339: 354-365
  • 82 Shah MM, Sakurai H, Gallegos TF. et al. Growth factor-dependent branching of the ureteric bud is modulated by selective 6-O sulfation of heparin sulfate. Dev Biol. 2011; 356: 19-27
  • 83 Nigam SK, Bush KT. Growth factor-heparan sulfate “switches” regulating stages of branching morphogenesis. Pediatr Nephrol. 2014; 29: 727-735
  • 84 Halt K, Vainio S. Coordination of kidney organogenesis by WNT signaling. Pediatr Nephrol. 2014; 29: 737-744
  • 85 Luz M, Spanni-Müller S, Özhan G. et al. Dynamic association with donor cell filopodia and lipid-modification are essential features of wnt8a, during patterning of the zebrafish. PLoS One 2014; 9: e84922
  • 86 Stanganello E, Hagemann Al, Mattes B. et al. Filopodia-based Wnt transport during vertebrate tissue patterning. Nat Commun 2015; 6: 5846
  • 87 Hsiung F, Ramirez-Weber FA, Iwaki DD. et al. Dependence of Drosophila wing immaginal dis cytonemes on decapentaplegic. Nature 2005; 437: 560-563
  • 88 Gill PS, Rosenblum ND. Control of murine kidney development by sonic hedgehog and its GLI effectors. Cell Cycle. 2006; 5: 1426-1430
  • 89 Bischoff M, Gradilla AC, Seijo I. et al. Cytonemes are required for the establishment of a normal Hedgehog morphogen gradient in Drosophila epithelia. Nat Cell Biol. 2013; 15: 1269-1281
  • 90 Sanders TA, Llagostatera E, Barna M. Specialized filopodia direct long-range transport of SSH during vertebrate tissue patterning. Nature 2013; 497: 628-632
  • 91 Liu Z, Shi H, Szymczak LC. et al. Promotion of bone morphogenetic protein signaling by tetraspins and glycosingolipids. PLos Genet. 2015; 11: e1005221
  • 92 Inaba M, Buszczak M, Yamashita YM. Nanotubes mediate niche-stem-cell signaling in the drosophila testis. Nature 2015; 523: 329-332
  • 93 Gurke S, Barroso JFV, Gerdes HH. The art of cellular communication: tunneling nanotubes bridge the divide. Histochem Cell Biol 2008; 129: 539-550
  • 94 Kimura S, Hase K, Ohno H. The molecular basis of induction and formation of tunneling nanotubes. Cell Tissue Res. 2013; 352: 67-76
  • 95 Gerdes HH, Pepperkok R. Cell-to-cell communication: current views and future perspectives. Cell Tissue Res. 2013; 352: 1-3
  • 96 Austefjord MW, Gerdes HH, Wang X. Tunneling nanotubes: Diversity in morphology and structure. Comm Integr Biol 2014; 7: e27934
  • 97 Valente S, Rossi R, Resta L. et al. Exploring the human mesenchymal stem cell tubule communication network through electron microscopy. Ultrastruc Pathol 2015; 39: 88-94
  • 98 Abounit S, Delage E, Zurzolo C. Identification of tunneling nanotubes for intercellular trafficking. Curr Protoc Cell Biol 2015; 67: 12.10.1-12.10.21
  • 99 Plotnikov EY, Khryapenkova TG, Galina SI. et al. Cytoplasm and organelle transfer between mesenchymal potent stromal cells and renal tubular cells in co-culture. Exp Cell Res. 2010; 316: 2447-2455
  • 100 Benard M, Schapman D, Lebon A. et al. Structural and functional analysis of tunneling nanotubes (TnTs) using gCW STED and gconfocal approaches. Biol Cell. 2015; 107: 419-425
  • 101 Borges FT, Reis LA, Schor N. Extracellular vesicles: Structure, function, and potential clinical uses in renal diseases. Braz J Med Res 2013; 46: 824-830
  • 102 Bianchi F, Sala E, Donadei C. et al. Potential advantages of acute kidney injury management by mesenchymal stem cells. World J Stem Cells. 2014; 6: 644-650
  • 103 Camussi G, Deregibus MC, Tetta C. Paracrine/endocrine mechanism of stem cells on kidney repair: Role of microvesicle-mediated transfer of genetic information. Curr Opin Nephrol Hypertens. 2010; 19: 7-12
  • 104 Aggarwal S, Moggio A, Bussolati B. Concise review: Stem/progenitor cells for renal repair : current knowledge and perspectives. Stem Cells Transl Med 2013; 2: 1011-1019
  • 105 Holthöfer H. Vascularization of the embryonic kidney. Detection of endothelial cells with Ulex europaeus I lectin. Cell Diff 1987; 20: 27-31
  • 106 Kloth S, Ebenbeck C, Monzer J. et al. Three-dimensional organization of the developing vasculature of the kidney. Cell Tissue Res. 1997; 287: 193-201
  • 107 Han KH, Lim JM, Kim MY. et al. Expression of endothelial nitric oxide synthase in developing rat kidney. Am J Physiol Renal Physiol 2005; 288: F694-F702
  • 108 Rymer C, Paredes J, Halt K. et al. Renal blood flow and oxygenation drive nephron progenitor differentiation. Am J Physiol Renal Physiol 2014; 307: F337-F345
  • 109 Nemolato S, Cabras T, Messana I. et al. Do β-thymosins play a role in human nephrogenesis?. In: Fa G, Fanos V. eds. Kidney development in renal pathology. Berlin: Springer; 2014: 81-94
  • 110 Mora CA, Baumann CA, Paino JE. et al. Biodistribution of synthetic thymosin beta 4 in the serum, urine, and major organs in mice. Int J Immunopharmacol. 1997; 19: 1-8
  • 111 Pina AL, Kubitza M, Brawanski A. et al. Expression of pigment-epithelium-derived factor during kidney development and aging. Cell Tissue Res. 2007; 329: 329-338
  • 112 Kitamoto Y, Tokunaga H, Tomita K. Vascular endothelial growth factor is an essential molecule for mouse kidney development: glomerulogenesis and nephrogenesis. J Clin Invest. 1997; 99: 2351-2357
  • 113 Marlier A, Schmidt-Ott KM, Gallagher AR. et al. Vegf as an epithelium morphogen modulates branching morphogenesis of embryonic kidney by direct acting on the ureteric bud. Mech Dev. 2009; 126: 91-98
  • 114 Schley G, Scholz H, Kraus A. et al. Hypoxia inhibits nephrogenesis through paracrine Vegfa despite the ability to enhance tubulogenesis. Kidney Int. 2015; 88: 1283-1292
  • 115 Halt KJ, Pärssinen HE, Juntilla SM. et al. CD146(+) cells are essential for kidney vasculare development. Kidney Int. 2016; 90: 311-324
  • 116 Machura K, Steppan D, Neubauer B. et al. Developmental renin expression in mice with defective renin-angiotensin system. Am J Physiol Renal Physiol 2009; 297: F1371-F1380
  • 117 Yosypiv IV. Renin-angiotensin system in the ureteric bud branching morphogenesis: Implications for kidney disease. Pediatr Nephrol. 2014; 29: 609-620
  • 118 Song R, Preston G, Kidd L. et al. Prorenin receptor is critical for nephron progenitors. Dev Biol. 2016; 409: 382-391
  • 119 Neubauer B, Machura K, Schnermann J. et al. Renin expression in large renal vessels during fetal development depends on functional beta1/beta2-adrenergic receptors. Am J Physiol Renal Physiol 2011; 301: F71-F77
  • 120 Sariola S, Ekblom P, Henke-Fahle S. Embryonic neurons as in vitro inducers of differentiation of nephrogenic mesenchyme. Dev Biol. 1989; 132: 271-281
  • 121 Ola R, Jakobson M, Kvist J. et al. The GDNF target Vsnl1 marks the ureteric tip. J Am Soc Nephrol. 2011; 22: 274-284
  • 122 Zanni G, Michno W, Di Martino E. et al. Lithium accumulates in neurogenic brain regions as revealed by high resolution ion imaging. Sci Rep 2017; 7: 40726
  • 123 Davies JA, Garrod DR. Induction of early stages of kidney tubule differentiation by lithium ions. Dev Biol. 1995; 167: 50-60
  • 124 Jope RS. Lithium and GSK-3: one inhibitor, two inhibitory actions, multiple outcomes. Trends Pharmacol Sci. 2003; 24: 441-443
  • 125 Kuure S, Popsueva A, Jakobson M. et al. Glycogen synthase kinase-3 inactivation and stabilization of beta-catenin induce nephron differentiation in isolated mouse and rat kidney mesenchymes. J Am Soc Nephrol. 2007; 18: 1130-1139
  • 126 Ye S, Tan L, Yang R. et al. Pleiotropy of glycogen synthase kinase-3 inhibition by CHIR99021 promotes self-renewal of embryonic stem cells from refractory mouse strains. PLoS One 2012; 7: e35892
  • 127 Araoka T, Mae S, Kurose Y. et al. Efficient and rapid induction of human iPSCs/ESCs into nephrogenic intermediate mesoderm using small molecule based differentiation methods. PLoS One 2014; 9: e84881
  • 128 Lam AQ, Freedman BS, Morizane R. et al. Rapid and efficient differentiation of human pluripotent stem cells into intermediate mesoderm that forms tubules expressing kidney proximal tubular markers. J Am Soc Nephrol. 2014; 25: 1211-1225
  • 129 Thesleff I, Ekblom P. Role of transferrin in branching morphogenesis, growth and differentiation of the embryonic kidney. J Embryol Exp Morphol 1984; 82: 147-161
  • 130 Li JY, Paragas N, Ned RM. et al. Scara5 is a ferritin receptor mediating non-transferrin iron delivery. Dev Cell. 2009; 16: 35-46
  • 131 Minuth WW. The rabbit nephrogenic zone in culture: past, present and future as a model to investigate causes of impaired nephrogenesis. J Pediatric Neonatal Individualized Medicine 2017; 6: e060111