From kidney development to drug delivery and tissue engineering strategies in renal regenerative medicine

Deterioration of renal function is typically slow but progressive, and therefore renal disease is often diagnosed in a late stage when already serious complaints occur. Ultimately when renal function has dropped below 10%, renal replacement is required. Renal transplantation provides a long-term sol...

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Published inJournal of controlled release Vol. 152; no. 1; pp. 177 - 185
Main Authors Dankers, Patricia Y.W., Boomker, Jasper M., Meijer, E.W., Popa, Eliane R., van Luyn, Marja J.A.
Format Journal Article Conference Proceeding
LanguageEnglish
Published Kidlington Elsevier B.V 30.05.2011
Elsevier
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Abstract Deterioration of renal function is typically slow but progressive, and therefore renal disease is often diagnosed in a late stage when already serious complaints occur. Ultimately when renal function has dropped below 10%, renal replacement is required. Renal transplantation provides a long-term solution but due to shortage of donor kidneys most patients receive hemodialysis therapy. Although hemodialysis is an effect method to correct disturbances in water and electrolyte balances in the body, it does not substitute for the important endocrine and metabolic renal functions that are critical for homeostasis. Among these functions are, the renal production of renin which controls blood pressure, the secretion of erythropoietin which stimulates the synthesis of red blood cells, and the excretion of protein bound waste products. As a consequence, many dialysis patients remain in poor health. With the development of regenerative medicine, and particularly tissue engineering and novel drug delivery strategies, alternative routes for renal replacement are emerging. Increasing understanding of (stem) cells, growth factors and regeneration in the kidney has contributed to a whole new view on restoration and reconstruction of (parts of) renal tissue that may be used to improve current renal replacement therapies. Here, an overview of critical interactions between cells, growth factors and extracellular matrix molecules in kidney development and regeneration will be described. Ultimately, we will discuss how these interactions can be translated to strategies for in-vivo regeneration and in-vitro reconstruction of the kidney. Alternative routes for kidney replacement are emerging with the development of regenerative medicine, and particularly tissue engineering and novel drug delivery strategies. A combination of cells, factors and materials is used. [Display omitted]
AbstractList Deterioration of renal function is typically slow but progressive, and therefore renal disease is often diagnosed in a late stage when already serious complaints occur. Ultimately when renal function has dropped below 10%, renal replacement is required. Renal transplantation provides a long-term solution but due to shortage of donor kidneys most patients receive hemodialysis therapy. Although hemodialysis is an effect method to correct disturbances in water and electrolyte balances in the body, it does not substitute for the important endocrine and metabolic renal functions that are critical for homeostasis. Among these functions are, the renal production of renin which controls blood pressure, the secretion of erythropoietin which stimulates the synthesis of red blood cells, and the excretion of protein bound waste products. As a consequence, many dialysis patients remain in poor health. With the development of regenerative medicine, and particularly tissue engineering and novel drug delivery strategies, alternative routes for renal replacement are emerging. Increasing understanding of (stem) cells, growth factors and regeneration in the kidney has contributed to a whole new view on restoration and reconstruction of (parts of) renal tissue that may be used to improve current renal replacement therapies. Here, an overview of critical interactions between cells, growth factors and extracellular matrix molecules in kidney development and regeneration will be described. Ultimately, we will discuss how these interactions can be translated to strategies for in-vivo regeneration and in-vitro reconstruction of the kidney.
Deterioration of renal function is typically slow but progressive, and therefore renal disease is often diagnosed in a late stage when already serious complaints occur. Ultimately when renal function has dropped below 10%, renal replacement is required. Renal transplantation provides a long-term solution but due to shortage of donor kidneys most patients receive hemodialysis therapy. Although hemodialysis is an effect method to correct disturbances in water and electrolyte balances in the body, it does not substitute for the important endocrine and metabolic renal functions that are critical for homeostasis. Among these functions are, the renal production of renin which controls blood pressure, the secretion of erythropoietin which stimulates the synthesis of red blood cells, and the excretion of protein bound waste products. As a consequence, many dialysis patients remain in poor health. With the development of regenerative medicine, and particularly tissue engineering and novel drug delivery strategies, alternative routes for renal replacement are emerging. Increasing understanding of (stem) cells, growth factors and regeneration in the kidney has contributed to a whole new view on restoration and reconstruction of (parts of) renal tissue that may be used to improve current renal replacement therapies. Here, an overview of critical interactions between cells, growth factors and extracellular matrix molecules in kidney development and regeneration will be described. Ultimately, we will discuss how these interactions can be translated to strategies for in-vivo regeneration and in-vitro reconstruction of the kidney. Alternative routes for kidney replacement are emerging with the development of regenerative medicine, and particularly tissue engineering and novel drug delivery strategies. A combination of cells, factors and materials is used. [Display omitted]
Author van Luyn, Marja J.A.
Dankers, Patricia Y.W.
Meijer, E.W.
Boomker, Jasper M.
Popa, Eliane R.
Author_xml – sequence: 1
  givenname: Patricia Y.W.
  surname: Dankers
  fullname: Dankers, Patricia Y.W.
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  givenname: Eliane R.
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  fullname: Popa, Eliane R.
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  givenname: Marja J.A.
  surname: van Luyn
  fullname: van Luyn, Marja J.A.
  organization: Department of Pathology and Medical Biology, Stem Cells and Tissue Engineering Group, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands
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Issue 1
Keywords Growth factor delivery
Membrane
Regenerative medicine
Supramolecular polymer
Kidney development
Bioartificial kidney
Performance evaluation
Drug
Delivery system
Pharmaceutical technology
Tissue engineering
Polymer
Drug carrier
Research and development
Kidney
Growth factor
Language English
License CC BY 4.0
Copyright © 2011 Elsevier B.V. All rights reserved.
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Snippet Deterioration of renal function is typically slow but progressive, and therefore renal disease is often diagnosed in a late stage when already serious...
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SubjectTerms Animals
Bioartificial kidney
Biological and medical sciences
Blood pressure
Cell Adhesion Molecules - physiology
Controlled release
dialysis
Drug delivery
Drug Delivery Systems
drugs
electrolytes
Erythrocytes
Erythropoietin
Excretion
Extracellular matrix
Extracellular Matrix - physiology
General pharmacology
Growth factor delivery
Growth factors
Hemodialysis
Homeostasis
Humans
Kidney - anatomy & histology
Kidney - embryology
Kidney - physiology
Kidney development
Kidney diseases
kidney transplant
Kidney transplantation
kidneys
Medical sciences
Membrane
patients
Pharmaceutical technology. Pharmaceutical industry
Pharmacology. Drug treatments
Regeneration
Regenerative Medicine
Renal function
Renal Replacement Therapy
Renin
Reviews
Secretion
Signal Transduction
Supramolecular polymer
Tissue Engineering
Wastes
Title From kidney development to drug delivery and tissue engineering strategies in renal regenerative medicine
URI https://dx.doi.org/10.1016/j.jconrel.2011.01.034
https://www.ncbi.nlm.nih.gov/pubmed/21334390
https://search.proquest.com/docview/1014103988
https://search.proquest.com/docview/871001914
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