Pregled bibliografske jedinice broj: 897399
A histological analysis of glycogen content in hepatocytes of trefoil factor family 2 and trefoil factor family 3 knock-out mice
A histological analysis of glycogen content in hepatocytes of trefoil factor family 2 and trefoil factor family 3 knock-out mice // 13th Multinational Congress on Microscopy: Book of Abstracts / Weber, Igor ; Tolić, Iva ; Kovačević, Goran ; Vidoš, Ana (ur.).
Zagreb, 2017. str. 335-335 (poster, nije recenziran, sažetak, stručni)
CROSBI ID: 897399 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A histological analysis of glycogen content in
hepatocytes of trefoil factor family 2 and
trefoil factor family 3 knock-out mice
Autori
Rođak, Edi ; Ivić, Kristina ; Belovari, Tatjana ; Lovrić, Ivana ; Bijelić, Nikola ; Baus Lončar, Mirela
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
13th Multinational Congress on Microscopy: Book of Abstracts
/ Weber, Igor ; Tolić, Iva ; Kovačević, Goran ; Vidoš, Ana - Zagreb, 2017, 335-335
ISBN
978-953-7941-19-2
Skup
13th Multinational Congress on Microscopy
Mjesto i datum
Rovinj, Hrvatska, 24.09.2017. - 29.09.2017
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
Tff ; liver ; histology ; glycogen
Sažetak
Trefoil factor family (Tff) peptide 2 and Tff peptide 3 are small peptides mostly present in the gastrointestinal mucosa and related to mucosal protection and restitution. Tff3 is included in hepatic glucose metabolism, and both Tff2 and Tff3 peptide stimulate beta-cell proliferation in the pancreatic islets. Tff2 and Tff3 deficient mice including appropriate wild type mice of mixed background (Sv129/C57Bl6) (N=6 per genotype) were kept on standard diet until 6 month old. Glycogen distribution was monitored in PAS stained formalin fixed and paraffin embedded tissue sections (6 µm). Areas of strongest glycogen staining were chosen for analysis and glycogen- positive cells were counted within regions of 100 cells. Using an arbitrary semiquantitative scale, the signal was classified as weak (0-35 positive cells), medium (36-70 positive cells) and strong (71 or more positive cells). Tff3 deficient mice had the strongest accumulation of glycogen that was statistically increased compared to wild-type mice (p=0.005, Mann- Whitney U test). Liver glycogen distribution in Tff2 deficient mice was heterogeneous and overall signal did not differ statistically from that of wild-type mice (p=0.5). Our results support the notion that Tff3 peptide is included in the hepatic glucose and glycogen metabolism. Further, metabolism-oriented studies are needed to elucidate the exact metabolic role of Tff3 peptide.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
219-0982914-2179 - Uloga malih zaštitinih TFF proteina u zdravlju i bolesti (Belovari, Tatjana, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Medicinski fakultet, Osijek
Profili:
Mirela Baus Lončar
(autor)
Ivana Ilić
(autor)
Edi Rođak
(autor)
Tatjana Belovari
(autor)
Nikola Bijelić
(autor)