In many physiological processes such as the maintenance of homeostasis, the excretion of nitrogen catabolism waste and the secretion of endocrine factors. In renal pathology and injury, all these processes are altered and accompanied by several symptoms: hypertension due to the alteration of the renin/angiotensin system and/or an 58-49-1 imbalance of calcium and phosphorus metabolism induced by the deficiency of calcitriol [1]. Studying these pathophysiological mechanisms requires the use of in vitro models such as renal cell cultures. This methodology is limited by the complexity of the nephron, which consists of the glomerulus and various A196 site tubular segments (the proximal and distal tubules and collecting duct) and by the cellular heterogeneity of these segments, which comprise 15 types of epithelial cells with different properties and functions [2]. Among the different celltypes, proximal tubular epithelial cells (PT cells) play a major role in the reabsorption of substances such as glucose and amino acids and the control of acid-base balance by the excretion of almost all the bicarbonate and the synthesis of ammonia [3]. They are also involved in the excretion of metabolic end products [4]. Furthermore PT cells are particularly sensitive to ischemic injury, and represent a primary target for xenobiotics, such as nephrotoxins (and 16985061 their metabolites), whose effects can extend up to the kidney failure [5,6]. To further elucidate the mechanisms of proximal tubular cell physiology and pathophysiology, as well as to study the potential mechanisms underlying nephrotoxins-induced renal toxicity, the primary culture of human proximal tubular cells represents a valuable tool [4,7,8]. Several techniques have been developed in order to establish such primary cultures: micro-dissection, enzymatic dissociation, the use of selective culture media, immunomagnetic cell sortingPrimary Human Proximal Renal Culture ModelFigure 1. Sorting proximal tubular cells using specific antibodies. (A) Fluorescence plot showing cells labeled with antibodies against CD10 (APC: allophycocyanin) and CD13 (PE: phycoerythrin). FACS analysis revealed about 4 double-positive cells. (B) Fluorescence plot 23148522 showing cells treated with isotypes to both antibodies to determine the upper threshold for non-specific fluorescence. doi:10.1371/journal.pone.0066750.gand isopycnic centrifugation [2,4,8?0]. However, only a few studies have verified the stability and differentiation status of these cells over time [2,11]. In fact, one study has shown the likely transdifferentiation, and the loss of specific markers, of primary renal tubule cells such as human distal tubular epithelial cells [12]. The main goal of this work was therefore to develop primary cultures of human renal proximal tubular epithelial cells and to ensure the stability and differentiation status of these cells over several passages.constitutional genetic characterization, only a verbal informed no-opposition for the use of tissue sample for research purpose is necessary according to the recommendations of the Haute Autorite de la Sante and the Code de la Sante Publique (Art ???L1211-2). This verbal consent was collected by the referring physician and notified on a special form in the patient record. For each surgical specimen, the absence of patient opposition was systematically verified and transmitted by the referring physician prior to the beginning of the cell isolation procedure. All tissue samples were de-indentified by.In many physiological processes such as the maintenance of homeostasis, the excretion of nitrogen catabolism waste and the secretion of endocrine factors. In renal pathology and injury, all these processes are altered and accompanied by several symptoms: hypertension due to the alteration of the renin/angiotensin system and/or an imbalance of calcium and phosphorus metabolism induced by the deficiency of calcitriol [1]. Studying these pathophysiological mechanisms requires the use of in vitro models such as renal cell cultures. This methodology is limited by the complexity of the nephron, which consists of the glomerulus and various tubular segments (the proximal and distal tubules and collecting duct) and by the cellular heterogeneity of these segments, which comprise 15 types of epithelial cells with different properties and functions [2]. Among the different celltypes, proximal tubular epithelial cells (PT cells) play a major role in the reabsorption of substances such as glucose and amino acids and the control of acid-base balance by the excretion of almost all the bicarbonate and the synthesis of ammonia [3]. They are also involved in the excretion of metabolic end products [4]. Furthermore PT cells are particularly sensitive to ischemic injury, and represent a primary target for xenobiotics, such as nephrotoxins (and 16985061 their metabolites), whose effects can extend up to the kidney failure [5,6]. To further elucidate the mechanisms of proximal tubular cell physiology and pathophysiology, as well as to study the potential mechanisms underlying nephrotoxins-induced renal toxicity, the primary culture of human proximal tubular cells represents a valuable tool [4,7,8]. Several techniques have been developed in order to establish such primary cultures: micro-dissection, enzymatic dissociation, the use of selective culture media, immunomagnetic cell sortingPrimary Human Proximal Renal Culture ModelFigure 1. Sorting proximal tubular cells using specific antibodies. (A) Fluorescence plot showing cells labeled with antibodies against CD10 (APC: allophycocyanin) and CD13 (PE: phycoerythrin). FACS analysis revealed about 4 double-positive cells. (B) Fluorescence plot 23148522 showing cells treated with isotypes to both antibodies to determine the upper threshold for non-specific fluorescence. doi:10.1371/journal.pone.0066750.gand isopycnic centrifugation [2,4,8?0]. However, only a few studies have verified the stability and differentiation status of these cells over time [2,11]. In fact, one study has shown the likely transdifferentiation, and the loss of specific markers, of primary renal tubule cells such as human distal tubular epithelial cells [12]. The main goal of this work was therefore to develop primary cultures of human renal proximal tubular epithelial cells and to ensure the stability and differentiation status of these cells over several passages.constitutional genetic characterization, only a verbal informed no-opposition for the use of tissue sample for research purpose is necessary according to the recommendations of the Haute Autorite de la Sante and the Code de la Sante Publique (Art ???L1211-2). This verbal consent was collected by the referring physician and notified on a special form in the patient record. For each surgical specimen, the absence of patient opposition was systematically verified and transmitted by the referring physician prior to the beginning of the cell isolation procedure. All tissue samples were de-indentified by.
