Ask a Librarian

Threre are lots of ways to contact a librarian. Choose what works best for you.

HOURS TODAY

10:00 am - 4:00 pm

Reference Desk

CONTACT US BY PHONE

(802) 656-2022

Voice

(802) 503-1703

Text

MAKE AN APPOINTMENT OR EMAIL A QUESTION

Schedule an Appointment

Meet with a librarian or subject specialist for in-depth help.

Email a Librarian

Submit a question for reply by e-mail.

WANT TO TALK TO SOMEONE RIGHT AWAY?

Library Hours for Thursday, November 21st

All of the hours for today can be found below. We look forward to seeing you in the library.
HOURS TODAY
8:00 am - 12:00 am
MAIN LIBRARY

SEE ALL LIBRARY HOURS
WITHIN HOWE LIBRARY

MapsM-Th by appointment, email govdocs@uvm.edu

Media Services8:00 am - 7:00 pm

Reference Desk10:00 am - 4:00 pm

OTHER DEPARTMENTS

Special Collections10:00 am - 6:00 pm

Dana Health Sciences Library7:30 am - 11:00 pm

 

CATQuest

Search the UVM Libraries' collections

UVM Theses and Dissertations

Browse by Department
Format:
Online
Author:
Lundberg, Allie Lynn
Dept./Program:
Animal and Veterinary Sciences
Year:
2019
Degree:
M.S.
Abstract:
Intraovarian growth factors play a vital role in influencing the fate of ovarian follicles. They affect proliferation versus apoptosis of granulosa cells (GCs), and can influence whether small antral follicles continue their growth or undergo atresia. Transforming Growth Factor-alpha (TGF[alpha]), an oocyte-derived growth factor, is thought to regulate granulosa cell function, yet has been largely overshadowed by current interest in TGF-beta superfamily members, such as bone morphogenetic proteins (BMPs) and anti-Mullerian hormone (AMH). In the current study, effects of TGF[alpha] on bovine GC proliferation, intracellular signaling and cytokine-induced apoptosis were evaluated. Briefly, all small antral follicles (3-5mm) from bovine ovaries were aspirated and the cells were initially plated in T25 flasks containing DMEM/F12 medium, 10% FBS, and antibiotic-antimycotic, and incubated at 37 degrees Celsius in 5% CO2 for 3-4 days. Once confluent, the cells were sub-cultured to 96-, 12- or 6-well plates in serum-free conditions (insulin 100 ng/mL; transferrin 55 ng/mL; sodium selenite 6.7 pg/mL). 24-hour treatment of bovine GCs with TGF[alpha] (10 and 100ng/mL) stimulated cell proliferation compared to control (p<0.05; n = 7 ovary pairs). Cell proliferation was accompanied by a concomitant increase in mitogen-activated protein kinase (MAPK) signaling within 2 hours of treatment, as measured by phosphorylated ERK1/2 expression (p<0.05, n = 3 ovary pairs). These effects were entirely negated, however, by the MAPK inhibitor, U0126 (10uM, p<0.05). Additionally, pre-exposure of the bovine GCs to TGF[alpha] (100ng/mL) failed to prevent Fas Ligand (100ng/mL)-induced apoptosis, as determined by caspase 3/7 activity (P<0.05, n = 7 ovary pairs). Collectively, the results indicate TGF[alpha] stimulates proliferation of bovine GCs from small antral follicles via a MAPK/ERK-mediated mechanism, but this action alone fails to prevent apoptosis, suggesting TGF[alpha] may be incapable of promoting the persistence of follicles during the process of follicular selection and deviation.