دورية أكاديمية

Podocytopathies

التفاصيل البيبلوغرافية
العنوان: Podocytopathies
المؤلفون: Peco-Antić Amira, Mulić Bilsana
المصدر: Srpski Arhiv za Celokupno Lekarstvo, Vol 148, Iss 9-10, Pp 631-636 (2020)
بيانات النشر: Serbian Medical Society, 2020.
سنة النشر: 2020
المجموعة: LCC:Medicine
مصطلحات موضوعية: steroid resistent nephrotyc syndrome, glomerulosclerosis, foot process effacement, mesenhimal-epithelilal transition, Medicine
الوصف: Podocytopathies include a wide spectrum of primary or secondary glomerular diseases that are the consequence of the podocyte injuries. The damage of podocytes can occur due to congenital or acquired disorders of podocyte transcriptional regulators, altered components of the slit diaphragm complex, abnormal assembly, or function of the actin-based cytoskeleton, dysfunction of membranes or cytoplasmic proteins, and mitochondrial injury. Podocytes reactions to injurious stimulus include FP effacement, apoptosis, and loss of podocyte, developmental arrest associated by mild proliferative activity, and dedifferentiation with moderated proliferation. Based on histopathological findings, podocytopathy may be diagnosed such as minimal change nephropathy; focal segmental glomerulosclerosis, diffuse mesangial sclerosis, or collapsing glomerulopathy while in relation to their etiology can be categorized as idiopathic, genetic, and reactive. Podocytopathies may be diagnosed due to podocyte morphological changes, immunohistochemistry, circulating and urine biomarkers, and genetic analysis. The primary clinical focus in prevention should be to reduce the factors that can damage the podocytes and cause hyperperfusion/hypertrophy of the glomerulus. Nowadays, control of systemic and intra glomerular hypertension by pharmacological blockade of angiotensin II is a central in the prevention strategy, while regeneration of podocytes by stem cells is therapeutic strategy of the future.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
Serbian
تدمد: 0370-8179
2406-0895
العلاقة: https://doaj.org/toc/0370-8179Test; https://doaj.org/toc/2406-0895Test
DOI: 10.2298/SARH181226067P
الوصول الحر: https://doaj.org/article/4b46bb550ee64d828da646a973c04d3aTest
رقم الانضمام: edsdoj.4b46bb550ee64d828da646a973c04d3a
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:03708179
24060895
DOI:10.2298/SARH181226067P