TY - UNPB
T1 - Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids
AU - Lindoso, Rafael Soares
AU - Yengej, Fjodor A. Yousef
AU - Voellmy, Franziska
AU - Altelaar, Maarten
AU - Juncosa, Estela Mancheno
AU - Tsikari, Theano
AU - Ammerlaan, Carola M.E.
AU - Balkom, Bas W.M. Van
AU - Verhaar, Marianne C.
AU - Masereeuw, Rosalinde
PY - 2022/2/9
Y1 - 2022/2/9
N2 - Advanced kidney in vitro models such as organoids or tubuloids still lack the intrinsic expression of various transport proteins needed for active secretory function. Extracellular vesicles (EVs), cell-derived structures that constitute the organ’s microenvironment, are known to regulate various cellular processes, including kidney development and regeneration across the nephron. In this study, we propose a new application of renal tubular epithelial cell EVs as modulators for tubuloid functional maturation by increasing the levels of various differentiation markers such as organic anion transport 1 (OAT1), a protein involved in endogenous waste excretion. First, we show that EVs from engineered proximal tubule cells increased the expression of several transcription factors and epithelial transporters in tubuloids that resulted in improved cellular transport capacity. Next, a more in-depth proteomic data analysis demonstrated that EVs can trigger various biological pathways, including mesenchymal-to-epithelial transition, which is crucial in the tubular epithelial maturation process. Moreover, we demonstrated that EV-treated tubuloid-derived cells in a 3D tubular conformation as part of a bioartificial kidney can generate a tight polarized epithelial monolayer with formation of dense cilia structures. In conclusion, EVs from renal tubular epithelial cells can phenotypically improve tubuloid maturation, thereby enhancing their potential as preclinical models and functional units in regenerative therapies.
AB - Advanced kidney in vitro models such as organoids or tubuloids still lack the intrinsic expression of various transport proteins needed for active secretory function. Extracellular vesicles (EVs), cell-derived structures that constitute the organ’s microenvironment, are known to regulate various cellular processes, including kidney development and regeneration across the nephron. In this study, we propose a new application of renal tubular epithelial cell EVs as modulators for tubuloid functional maturation by increasing the levels of various differentiation markers such as organic anion transport 1 (OAT1), a protein involved in endogenous waste excretion. First, we show that EVs from engineered proximal tubule cells increased the expression of several transcription factors and epithelial transporters in tubuloids that resulted in improved cellular transport capacity. Next, a more in-depth proteomic data analysis demonstrated that EVs can trigger various biological pathways, including mesenchymal-to-epithelial transition, which is crucial in the tubular epithelial maturation process. Moreover, we demonstrated that EV-treated tubuloid-derived cells in a 3D tubular conformation as part of a bioartificial kidney can generate a tight polarized epithelial monolayer with formation of dense cilia structures. In conclusion, EVs from renal tubular epithelial cells can phenotypically improve tubuloid maturation, thereby enhancing their potential as preclinical models and functional units in regenerative therapies.
KW - extracellular vesicles
KW - kidney tubuloids
KW - maturation
KW - organic anion transporter 1
KW - proteomics
KW - bioengineered kidney tubules
U2 - 10.1101/2022.02.08.479621
DO - 10.1101/2022.02.08.479621
M3 - Preprint
SP - 1
EP - 31
BT - Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids
PB - bioRxiv
ER -