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Immunohistochemical and Ultrastructural Characterization of Telocytes in Normal and Diabetic Human Kidneys

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Background: Telocytes are interstitial stromal cells identified in various human organs, including the kidney. Their presence and role in human diabetic kidney disease remain unknown. Methods: To identify and localize telocytes in glomerular and tubule-interstitial compartments, both normal and diabetic human renal tissues were examined using immunohistochemistry, immunofluorescence, and transmission electron microscopy. Results: Renal telocytes are elongated interstitial cells with long, thin telopodes, showing alternating thin and thick segments. They expressed CD34, Nestin, α-SMA, and Vimentin markers. Occasionally, c-Kit expression was observed in some rounded and spindle cells, while no positivity was detected for PDGFR-β and NG2. Telocytes were identified around Bowman’s capsule, tubules, and peritubular capillaries in both normal and diabetic conditions. In diabetic renal samples, there was a significant increase in α-SMA expressing telocytes, leading to periglomerular fibrosis. These telocytes also exhibited a synthetic phenotype with proteoglycan deposition in the extracellular matrix and, in some cases, showed pre-adipocytic differentiation. Conclusions: Telocytes were identified in normal and diabetic human kidneys. These cells form an elastic mechanical scaffold in the interstitium and are present in all renal cortical compartments. In diabetic samples, their increased α-SMA expression and synthetic phenotype suggest their potential role in the pathogenesis of diabetic nephropathy.
Title: Immunohistochemical and Ultrastructural Characterization of Telocytes in Normal and Diabetic Human Kidneys
Description:
Background: Telocytes are interstitial stromal cells identified in various human organs, including the kidney.
Their presence and role in human diabetic kidney disease remain unknown.
Methods: To identify and localize telocytes in glomerular and tubule-interstitial compartments, both normal and diabetic human renal tissues were examined using immunohistochemistry, immunofluorescence, and transmission electron microscopy.
Results: Renal telocytes are elongated interstitial cells with long, thin telopodes, showing alternating thin and thick segments.
They expressed CD34, Nestin, α-SMA, and Vimentin markers.
Occasionally, c-Kit expression was observed in some rounded and spindle cells, while no positivity was detected for PDGFR-β and NG2.
Telocytes were identified around Bowman’s capsule, tubules, and peritubular capillaries in both normal and diabetic conditions.
In diabetic renal samples, there was a significant increase in α-SMA expressing telocytes, leading to periglomerular fibrosis.
These telocytes also exhibited a synthetic phenotype with proteoglycan deposition in the extracellular matrix and, in some cases, showed pre-adipocytic differentiation.
Conclusions: Telocytes were identified in normal and diabetic human kidneys.
These cells form an elastic mechanical scaffold in the interstitium and are present in all renal cortical compartments.
In diabetic samples, their increased α-SMA expression and synthetic phenotype suggest their potential role in the pathogenesis of diabetic nephropathy.

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