Abstract
The human body is a highly sophisticated machine that is not fully understood to date. The body function is highly dependent on the versatile functions performed by different organs, which have their diverse arrangement of cells. Every organ (perhaps every body part) is prone to damage and malfunction because of the topological conditions, lifestyle, habitats, and food chemicals. Hel** humans to lead an easy, luxurious, and healthy life are the primary goal of any technology, especially extending human life is the ultimate target of medical instrumentation. The importance of develo** innovative techniques for disease diagnosis and treatment are burning topics since the start of the medical and pharmaceutical industry. Kidney failure is one of the common health issues worldwide, which is a slow poison affecting 10% of the world population. The importance of replacing the kidney is essential to extend a patient life. This review focuses on Organ-on-Chip technology with a major focus on Kidney-on-Chip (KOC). The evolution of techniques to diagnose and treat organ failure is elaborately presented. Major emphasis solely on the development of kidney failure causes, diagnostic techniques, replacement techniques are reported with a timeline of developments. The major functions of the kidney that have been achieved artificially so far are reviewed to the deepest level. The future directions in this field are predicted and presented. MEMS and microfluidics allow the design and manufacturing of devices at microscale without compromising the actual functionalities, especially in terms of disease diagnosis and treatment. Microfluidics technology revolutionized the development of artificial organ industry, the chances of realizing an organ substantially improved.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Jang, K.J., Suh, K.Y.: A multi-layer microfluidic device for efficient Culture and analysis of renal tubular cells. Lab Chip 10, 36–42 (2010)
Maschmeyer, I., Lorenz, A.K., Schimek, K., Hasenberg, T., Ramme, A.P., Hubner, J., Lindner, M., Drewell, C., Bauer, S., Thomas, A., Sambo, N.S., Sonntag, F., Lauster, R., Marx, U.: A four-organ-chip for interconnected long-term co-culture of human intestine, liver, skin and kidney equivalents. Lab Chip 15, 2688–2699 (2015)
Kimura, H., Yamamoto, T., Sakai, H., Sakai, Y., Fujii, T.: An integrated microfluidic system for long-term perfusion culture and on-line monitoring of intestinal tissue models. Lab Chip 8, 741–746 (2008)
Huh, D., Matthews, B.D., Mammoto, A., Montoya-Zavala, M., Hsin, H.Y., Ingber, D.E.: Reconstituting organ-level lung functions on a chip. Science 328, 1662–1668 (2010)
Tsai, M., Kita, A., Leach, J., Rounsevell, R., Huang, J.N., Moake, J., Ware, R.E., Fletcher, D.A., Lam, W.A.: In vitro modeling of the microvascular occlusion and thrombosis that occur in hematologic diseases using microfluidic technology. J. Clin. Invest. 122, 408–418 (2012)
Walsh, C.L., Babin, B.M., Kasinskas, R.W., Foster, J.A., McGarry, M.J., Forbes, N.S.: A multipurpose microfluidic device designed to mimic micro-environment gradients and develop targeted cancer therapeutics. Lab Chip 9, 545–554 (2009)
Torisawa, Y.S., Spina, C.S., Mammoto, T., Mammoto, A., Weaver, J.C., Tat, T., Collins, J.J., Ingber, D.E.: Bone marrow-on-a-chip replicates hematopoi-Eticniche physiology in-vitro. Nat. Methods 11, 663–669 (2014)
Zhang, C., Zhao, Z., Abdul Rahim, N.A., van Noort, D., Yu, H.: Lab Chip 9(22), 3185–3192 (2009)
Fitzpatrick S, Sprando R (2019) Advancing regulatory science through innovation: in vitro microphysiological systems. Cell. Mol. Gastroenterol. Hepatol. 7(1), 239
Liu, Y., Gill, E., Huang, Y.Y.S.: Microfluidic on-chip biomimicry for 3D cell culture: a ft-for-purpose investigation from the end user standpoint. Future Sci. OA 3(2), FSO173 (2017)
Williamson, A., Singh, S., Fernekorn, U., Schober, A.: The future of the patient-specific body-on-a-chip. Lab Chip 13, 3471–3480 (2013). https://doi.org/10.1039/c3lc50237fhttps://doi.org/10.1039/c3lc50237f
Kim, K., Ohashi, K., Utoh, R., Kano, K., Okano, T.: Preserved liver-specific functions of hepatocytes in 3D co-culture with endothelial cell sheets. Biomaterials 33, 1406–1413 (2012). https://doi.org/10.1016/j.biomaterials.2011.10.084https://doi.org/10.1016/j.biomaterials.2011.10.084
Xu, Y., Jang, K., Yamashita, T., Tanaka, Y., Mawatari, K., Kitamori, T.: Microchip-based cellular biochemical systems for practical applications and fundamental research: from microfluidics to nanofluidics. Anal. Bioanal. Chem. 402, 99–107 (2012). https://doi.org/10.1007/s00216-011-5296-5https://doi.org/10.1007/s00216-011-5296-5
El-Ali, J., Sorger, P.K., Jensen, K.F.: Cells on chips. Nature 442 (2006). https://doi.org/10.1038/nature05063
Bhushan, A., Martucci, N.J., Usta, O.B., Yarmush, M.L.: New technologies in drug metabolism and toxicity screening: organ-to-organ interaction. Expert Opin. Drug Metab. Toxicol. 12, 475–477 (2016). https://doi.org/10.1517/17425255.2016.1162292 (PMC free article)
Esch, E.W., Bahinski, A., Huh, D.: Organs-on-chips at the frontiers of drug discovery. Nat. Rev. Drug Discov. 14, 248–260 (2015). https://doi.org/10.1038/nrd4539[PMCfreearticle]https://doi.org/10.1038/nrd4539[PMCfreearticle]
Toh, Y.C., Lim, T.C., Tai, D., **ao, G., van Noort, D., Yu, H.: A microfluidic 3D hepatocyte chip for drug toxicity testing. Lab Chip 9, 2026–2035 (2009). https://doi.org/10.1039/b900912dhttps://doi.org/10.1039/b900912d
Ghaemmaghami, A.M., Hancock, M.J., Harrington, H., Kaji, H., Khademhosseini, A.: Biomimetic tissues on a chip for drug discovery. Drug Discov. Today 17, 173–181 (2012). https://doi.org/10.1016/j.drudis.2011.10.029https://doi.org/10.1016/j.drudis.2011.10.029
No, D.Y., Lee, K.H., Lee, J., Lee, S.H.: 3D liver models on a microplatform: well-defined culture, engineering of liver tissue and liver-on-a-chip. Lab Chip 15, 3822–3837 (2015). https://doi.org/10.1039/C5LC00611Bhttps://doi.org/10.1039/C5LC00611B
Nagrath, S., Sequist, L.V., Maheswaran, S., Bell, D.W., Irimia, D., Ulkus, L., Smith, M.R., Kwak, E.L., Digumarthy, S., Muzikansky, A., Ryan, P., Balis, U.J., Tompkins, R.G., Haber, D.A., Toner, M.: Isolation of rare circulating tumour cells in cancer patients by microchip technology. Nature 450 (2007)
Young, E.W.K.: Cells, tissues, and organs on chips: challenges and opportunities for the cancer tumor microenvironment. Integr. Biol. 5(9), 1096–1109 (2013). https://doi.org/10.1039/c3ib40076jhttps://doi.org/10.1039/c3ib40076j
Taylor, A.M., Blurton-Jones, M., Rhee, S.W., Cribbs, D.H., Cotman, C.W., Jeon, N.L.: A microfluidic culture platform for CNS axonal injury, regeneration and transport. Nat. Methods 2(8), 599 (2005)
Higgins, J.M., Eddington, D.T., Bhatia, S.N., Mahadevan, L.: Sickle cell vasoocclusion and rescue in a microfluidic device. PNAS 104(51), 20496–20500 (2007)
Joanne Wang, C., Li, X., Lin, B., Shim, S., Ming, G., Levchenko, A.: A microfluidics-based turning assay reveals complex growth cone responses to integrated gradients of substrate-bound ECM molecules and diffusible guidance cues. Lab Chip 8, 227–237 (2008)
McNamara, B.J., Diouf, B., Douglas-Denton, R.N., Hughson, M.D., Hoy, W.E., Bertram, J.F.: Comparison of nephron number, glomerular volume and kidney weight in Senegalese Africans and African Americans. Nephrol. Dial Transplant. 25, 1514–1520 (2010)
Manalich, A., Reyes, L., Herrera, M., Melendi, C., Fundora, I.: Relationship between weight at birth and the number and size of renal glomeruli in humans: a histomorphometric study. Kidney Int. 58, 770–777 (2000)
Jung, J.S., Preston, G.M., Smith, B.L., Gugginoll, W.B., Agre, P.: Molecular structure of the water channel through aquaporin CHIP. J. Biol. Chem. 269(20), 14648–14654 (1994)
Sateesh, J., Guha, K., Dutta, A., Sengupta, P., Agarwal, A., Srinivasa Rao, K.: Recreating the size dependent re-absorption function of proximal convoluted tubule towards artificial kidney applications-structural analysis and computational study. Artif. Organs (2020)
Baquet, A., Gaussin, V., Bollen, M., Stalmans, W., Hue, L.: Mechanism of activation of liver acetyl-CoA carboxylase by cell swelling. Eur. J. Biochem. FEBS 217, 1083–1089 (1993)
Peak, M., Al-Habori, M., Agius, L.: Regulation of glycogen synthesis and glycolysis by insulin, pH and cell volume. Interactions between swelling and alkalinization in mediating the effects of insulin. Biochem. J. 282(3), 797–805 (1992)
Hamill, O.P., Martinac, B.: Molecular basis of mechanotransduction in living cells. Physiol. Rev. 81, 685–740 (2001)
Davies, P.F.: Flow-mediated endothelial mechanotransduction. Physiol. Rev. 75, 519–560 (1995)
Traub, O., Berk, B.C.: Laminar shear stress: mechanisms by which endothelial cells transduce an atheroprotective force. Arterioscler. Thromb. Vasc. Biol. 18, 677–685 (1998)
Li, F., **e, X., Fan, J., Li, Z., Wu, J., Zheng, R.: Hydraulic pressure inducing renal tubular epithelial-myofibroblast transdifferentiation in vitro. J. Zhejiang Univ. Sci. B 10(9), 659–667 (2009)
Cai, Z., **n, J., Pollock, D.M., Pollock, J.S.: Shear stress-mediated NO production in inner medullary collecting duct cells. Am. J. Physiol. Renal. Physiol. 279, F270–F274 (2000)
Liu, W., Xu, S., Woda, C., Kim, P., Weinbaum, S., Satlin, L.M.: Effect of flow and stretch on the [Ca2+]i response of principal and intercalated cells in cortical collecting duct. Am. J. Physiol. Renal. Physiol. 285, F998–F1012 (2003)
Schnermann, J., Wahl, M., Liebau, G., Fischbach, H.: Balance between tubular flow rate and net fluid reabsorption in the proximal convolution of the rat kidney. I. Dependency of reabsorptive net fluid flux upon proximal tubular surface area at spontaneous variations of filtration rate. Pflugers Arch. 304, 90–103 (1968)
Giebisch, G., Windhager, E.E.: Characterization of renal tubular transport of sodium chloride and water as studied in single nephrons. Am. J. Med. 34, 1–6 (1963)
Du, Z., et al.: Axial flow modulates proximal tubule NHE3 and H-ATPase activities by changing microvillus bending moments. Am. J. Physiol. Renal. Physiol. 290, F289–F296 (2006)
Malnic, G., Berliner, R.W., Giebisch, G.: Flow dependence of K+ secretion in cortical distal tubules of the rat. Am. J. Physiol. 256, F932–F941 (1989)
Satlin, L.M., Sheng, S., Woda, C.B., Kleyman, T.R.: Epithelial Na(+) channels are regulated by flow. Am. J. Physiol. Renal. Physiol. 280, F1010–F1018 (2001)
Du, Z., Duan, Y., Yan, Q.S., Weinstein, A.M., Weinbaum, S., Wang, T.: Mechanosensory function of microvilli of the kidney proximal tubule. PNAS 101(35), 13068–13073 (2004)
Jha, V., Garcia-Garcia, G., Iseki, K., Li, Z., Naicker, S., Plattner, B., Saran, R., Wang, A.M., Yang, C.W.: Chronic kidney disease: global dimension and perspectives. Lancet 382(9888), 260–272 (2013)
Jang, K.-J., Mehr, A.P., Hamilton, G.A., McPartlin, L.A., Chung, S., Suh, K.-Y., Ingber, D.E.: Human kidney proximal tubule-on-a-chip for drug transport and nephrotoxicity assessment. Integr. Biol. 5, 1119 (2013)
Weia, Z., Amponsah, P.K., Al-Shatti, M., Nie, Z., Bandyopadhyay, B.: Engineering of polarized tubular structures in a microfluidic device to study calcium phosphate stone formation. Lab Chip 12(20), 4037–4040 (2012)
Kensinger, C., et al.: First implantation of silicon nanopore membrane hemofilters. ASAIO J. (Am. Soc. Artif. Inter. Org. 1992) 62(4), 491–495 (2016). https://doi.org/10.1097/MAT.0000000000000367
Suwanpayak, N., Jalil, M.A., Aziz, M.S., Ismail, F.D., Ali, J., Yupapin, P.P.: Blood cleaner on-chip design for artificial human kidney manipulation. Int. J. Nanomed. 6, 957–964 (2011)
Liu, W., Murcia, N.S., Duan, Yi., Weinbaum, S., Yoder, B.K., Schwiebert, E., Satlin, L.M.: Mechanoregulation of intracellular Ca2 concentration is attenuated in collecting duct of monocilium-impaired orpk mice. Am. J. Physiol. Renal. Physiol. 289, F978–F988 (2005)
Wang, L., Tao, T., Su, W., Yu, H., Yu, Y., Qin, J.: A disease model of diabetic nephropathy in a glomerulus-on-a-chip microdevice. Lab Chip 17(10), 1749–1760 (2017)
Zhou, M., et al.: Development of a functional glomerulus at the organ level on a chip to mimic hypertensive nephropathy. Sci. Rep. 6, 31771 (2016). https://doi.org/10.1038/srep31771
Weber, E.J., Chapron, A., Chapron, B.D., Voellinger, J.L., Lidberg, K.A., Yeung, C.K., Wang, Z., Yamaura, Y., Hailey, D.W., Neumann, T., Shen, D.D., Thummel, K.E., Muczynski, K.A., Himmelfarb, J., Kelly, E.J.: Development of a microphysiological model of human kidney proximal tubule function. Kidney Int. 90(3), 627–637 (2016). ISSN 0085-2538. https://doi.org/10.1016/j.kint.2016.06.011
Jang, K.-J., Mehr, A.P., Hamilton, G.A., McPartlin, L.A., Chung, S., Suh, K.-Y., Ingber, D.E.: Human kidney proximal tubule-on-a-chip for drug transport and nephrotoxicity assessment. Integr. Biol. 5(9), 1119–1129 (2013). https://doi.org/10.1039/c3ib40049b
Vriend, J., Nieskens, T.T.G., Vormann, M.K., et al.: Screening of drug-transporter interactions in a 3D microfluidic renal proximal tubule on a chip. AAPS J 20, 87 (2018). https://doi.org/10.1208/s12248-018-0247-0https://doi.org/10.1208/s12248-018-0247-0
Lin, N.Y.C., Homan, K.A., Robinson, S.S., Kolesky, D.B., Duarte, N., Moisan, A., Lewis, J.A.: Renal reabsorption in 3D vascularized proximal tubule models. Proc. Natl. Acad. Sci. 116(12), 5399–5404 (2019). https://doi.org/10.1073/pnas.1815208116
Weber, E.J., Chapron, A., Chapron, B.D., Voellinger, J.L., Lidberg, K.A., Yeung, C.K., Wang, Z., et al.: Development of a microphysiological model of human kidney proximal tubule function. Kidney Int. 90(3), 627–637 (2016)
Guha, K., Sateesh, J., Dutta, A., et al.: Mimicking kidney re-absorption using microfluidics by considering hydrostatic pressure inside kidney tubules: structural and analytical study. Microsyst. Technol. (2019). https://doi.org/10.1007/s00542-019-04720-9https://doi.org/10.1007/s00542-019-04720-9
Sateesh, J., Guha, K., Dutta, A., et al.: Regenerating re-absorption function of proximal convoluted tubule using microfluidics for kidney-on-chip applications. SN Appl. Sci. 2, 39 (2020). https://doi.org/10.1007/s42452-019-1840-2https://doi.org/10.1007/s42452-019-1840-2
Jang, K.-J., Cho, H.S., Kang, D.H., Bae, W.G., Kwon, T.-H., Suh, K.-Y.: Fluid-shear-stress-induced translocation of aquaporin-2 and reorganization of actin cytoskeleton in renal tubular epithelial cells. Integr. Biol. 3(2), 134–141 (2011)
Shum, H.C., Kim, J.-W., Weitz, D.A.: Microfluidic fabrication of monodisperse biocompatible and biodegradable polymersomes with controlled permeability. J. Am. Chem. Soc. 130(29), 9543–9549 (2008)
Friend, J., Yeo, L.: Fabrication of microfluidic devices using polydimethylsiloxane. Biomicrofluidics 4(2), 026502 (2010)
Ren, K., Zhou, J., Hongkai, Wu.: Materials for microfluidic chip fabrication. Acc. Chem. Res. 46(11), 2396–2406 (2013)
Lai, T.T., **e, D., Zhou, C.H., Cai, G.X.: Copper-catalyzed inter/intramolecular N-alkenylation of benzimidazoles via tandem processes involving selectively mild iodination of sp3 C-H bond at α-position of ester. J. Org. Chem. 81(19), 8806–8815 (2016)
**a, Y., Whitesides, G.M.: Soft lithography. Annu. Rev. Mater. Sci. 28(1), 153–184 (1998)
Whitesides, G.M., Ostuni, E., Takayama, S., Jiang, X., Ingber, D.E.: Soft lithography in biology and biochemistry. Annu. Rev. Biomed. Eng. 3(1), 335–373 (2001)
Kane, R.S., Takayama, S., Ostuni, E., Ingber, D.E., Whitesides, G.M.: Patterning proteins and cells using soft lithography. Biomaterials 20(23–24), 2363–2376 (1999)
Rogers, J.A., Nuzzo, R.G.: Recent progress in soft lithography. Mater. Today 8(2), 50–56 (2005)
Paul, M.T.Y., Kim, D., Saha, M.S., Stumper, J., Gates, B.D.: Patterning catalyst layers with microscale features by soft lithography techniques for proton exchange membrane fuel cells. ACS Appl. Energy Mater. (2020)
Kim, S.M., Leeb, S.H., Suh, K.Y.: Cell research with physically modified microfluidic channels: a review. Lab Chip 8, 1015–1023, 1015 (2008)
Striker, G.E., Striker, L.J.: Glomerular cell culture. Lab. Investig. J. Tech. Methods Pathol. 53(2), 122–131 (1985)
Tibbitt, M.W., Anseth, K.S.: Hydrogels as extracellular matrix mimics for 3D cell culture. Biotechnol. Bioeng. 103(4), 655–663 (2009)
Di Carlo, D., Wu, L.Y., Lee, L.P.: Dynamic single cell culture array. Lab on a Chip 6(11), 1445–1449 (2006)
Hung, P.J., Lee, P.J., Sabounchi, P., Lin, R., Lee, L.P.: Continuous perfusion microfluidic cell culture array for high-throughput cell-based assays. Biotechnol. Bioeng. 89(1), 1–8 (2005)
Nagy, A., Rossant, J., Nagy, R., Abramow-Newerly, W., Roder, J.C.: Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc. Natl. Acad. Sci. 90(18), 8424–8428 (1993)
Edmondson, R., Broglie, J.J., Adcock, A.F., Yang, L.: Three-dimensional cell culture systems and their applications in drug discovery and cell-based biosensors. Assay Drug Dev. Technol. 12(4), 207–218 (2014)
Mehling, M., Tay, S.: Microfluidic cell culture. Curr. Opin. Biotechnol. 25, 95–102 (2014)
Sung, J.H., Kam, C., Shuler, M.L.: A microfluidic device for a pharmacokinetic pharmacodynamics (PK-PD) model on a chip. Lab Chip 10, 446–455 (2010)
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2021 The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Sateesh, J., Guha, K., Dutta, A., Sengupta, P., Agarwal, A., Srinivasa Rao, K. (2021). Mimicking Human Kidney: Research Towards Better Solutions for Kidney Failure. In: Dutta, G., Biswas, A., Chakrabarti, A. (eds) Modern Techniques in Biosensors. Studies in Systems, Decision and Control, vol 327. Springer, Singapore. https://doi.org/10.1007/978-981-15-9612-4_14
Download citation
DOI: https://doi.org/10.1007/978-981-15-9612-4_14
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-15-9611-7
Online ISBN: 978-981-15-9612-4
eBook Packages: EngineeringEngineering (R0)