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Pregled bibliografske jedinice broj: 696239

Mechanism of cystogenesis in nephrotic kidneys: a histopathological study


Saraga, Marijan; Vukojević, Katarina; Krželj, Vjekoslav; Puretić, Zvonimir; Bočina, Ivana; Glavina Durdov, Merica; Weber, Stefanie; Dworniczak, Bernd; Galešić Ljubanović, Danica; Saraga-Babić, Mirna
Mechanism of cystogenesis in nephrotic kidneys: a histopathological study // BMC Nephrology, 15 (2014) doi:10.1186/1471-2369-15-3 (međunarodna recenzija, članak, znanstveni)


Naslov
Mechanism of cystogenesis in nephrotic kidneys: a histopathological study

Autori
Saraga, Marijan ; Vukojević, Katarina ; Krželj, Vjekoslav ; Puretić, Zvonimir ; Bočina, Ivana ; Glavina Durdov, Merica ; Weber, Stefanie ; Dworniczak, Bernd ; Galešić Ljubanović, Danica ; Saraga-Babić, Mirna

Izvornik
BMC Nephrology (1471-2369) 15 (2014);

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Nephrotic kidney; Cystogenesis; CNF; FSGS; Cell proliferation; Primary cilia; Apoptosis

Sažetak
Background: Nephrotic syndrome (NS) is pathological condition characterized by heavy proteinuria. Our study investigates hypothesis that change in cell proliferation of proximal tubules influences primary cilia structure and function and promotes cystogenesis in congenital nephrotic syndrome of the Finnish type (CNF) and focal segmental glomerulosclerosis (FSGS). Methods: CNF kidneys were analyzed genetically. Proliferation (Ki- 67), apoptosis (caspase-3), and primary cilia (α-tubulin) length and structure were analyzed immunohistochemically and ultrastructurally in healthy, CNF and FSGS kidneys. Cyst diameters were measured and correlated with proliferation index. Results: Proximal tubules cells of healthy kidneys did not proliferate. In nephrotic kidneys, tubules with apparently normal diameter covered by cuboidal/columnar epithelium (PTNC) contained 81.54% of proliferating cells in CNF and 36.18% in FSGS, while cysts covered with columnar epithelium (CC) contained 37.52% of proliferating cells in CNF and 45.23% in FSGS. The largest cysts, covered with squamous epithelium (CS) had 11.54% of proliferating cells in CNF and 13.76% in FSGS. Increase in cysts diameter correlated with changes in proliferation index, tubular cells shape, primary cilia formation and appearance of apoptotic cells. Conclusions: We present a novel histopathological data on the structure and possible changes in function of tubular cell in NS kidneys during cystogenesis. We suggest existence of common principles of cystogenesis in CNF and FSGS kidneys, including serious disturbances of tubular cells proliferation and apoptosis, and faulty primary cilia signaling leading to deterioration of proteinuria in NS kidneys.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Ustanove
KBC Split,
Prirodoslovno-matematički fakultet, Split,
Klinička bolnica "Dubrava",
Medicinski fakultet, Split

Časopis indeksira:


  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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