Impact of co-chaperone STIP1 expression in the pluripotency acquision induced by Oct4 in murine fibroblasts

• Grant number: 16/00440-9
• Support Opportunities: Scholarships abroad - Research
• Start date: August 08, 2016
• End date: February 07, 2017
• Field of knowledge: Biological Sciences - Morphology - Cytology and Cell Biology
• Principal Investigator: Marilene Hohmuth Lopes
• Grantee: Marilene Hohmuth Lopes
• Host Investigator: Marco Antonio Maximo Prado
• Host Institution: Instituto de Ciências Biomédicas (ICB). Universidade de São Paulo (USP). São Paulo , SP, Brazil
• Institution abroad: Western University , Canada

Abstract

Pluripotent cell have the potential to differentiate into all of the cell typesof an animal. This unique cell state is governed by an interconnected network of transcription factors, being Oct4 a central player in pluripotency induction and maintenance. Evidence pointed out to the participation of proteostase machinary regulated by co-chaperone STIP1 (Stress Inducible Phosphoprotein 1) and its partners, Hsp70 e Hsp90, in the embryogenesis and maintenance of pluripotent stem cells. Our data have revealed that STIP1 silencing impairs the pluripotent status of embryonic stem cells decreasing the expression of multiple transcription factors, including Oct4, Sox2, Nanog and STAT3. Interestingly, literature findings showed that Hsp90 is able to maintain stable the levels of pluripotency transcription factors, particularly, Oct4. Indeed, a depth study aimed the role of STIP1 and its partners in the regulation and maintenance of pluripotency is crucial to understanding the basic mechanisms that control stem cell pluripotency. Thus, the main goal of this proposal is to evaluate the role of STIP1 in the regulation of Oct4 expression in murine fibroblasts derived from transgenic mice expressing different STIP1 levels (wild-type, haploinsufficient and overexpressing STIP1) and a truncate isoform (deletion mutant for TPR1, the Hsp70 binding site) and consequently, to evaluate their participation in pluripotent state induction. Hence, dissecting the molecular basic of the stem cell pluripotency is essential to understand the biology of stem cells, the early embryonic developing and for clinical application in regenerative medicine. (AU)

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

LACKIE, RACHEL E.; RAZZAQ, ABDUL R.; FARHAN, SALI M. K.; QIU, LILY R.; MOSHITZKY, GILLI; BERALDO, FLAVIO H.; LOPES, MARILENE H.; MACIEJEWSKI, ANDRZEJ; GROS, ROBERT; FAN, JUE; et al. Modulation of hippocampal neuronal resilience during aging by the Hsp70/Hsp90 co-chaperone STI1. Journal of Neurochemistry, v. 153, n. 6, p. 32-pg., 2019-10-31. (16/00440-9, 17/20271-0)

LACKIE, RACHEL E.; RAZZAQ, ABDUL R.; FARHAN, SALI M. K.; QIU, LILY R.; MOSHITZKY, GILLI; BERALDO, FLAVIO H.; LOPES, MARILENE H.; MACIEJEWSKI, ANDRZEJ; GROS, ROBERT; FAN, JUE; et al. Modulation of hippocampal neuronal resilience during aging by the Hsp70/Hsp90 co-chaperone STI1. Journal of Neurochemistry, OCT 2019. (17/20271-0, 16/00440-9)

LIN, LILIAN TSAI-WEI; RAZZAQ, ABDUL; DI GREGORIO, SONJA E.; HONG, SOOJIE; CHARLES, BRENDAN; LOPES, MARILENE H.; BERALDO, FLAVIO; PRADO, VANIA F.; PRADO, MARCO A. M.; DUENNWALD, MARTIN L.. Hsp90 and its co-chaperone Sti1 control TDP-43 misfolding and toxicity. FASEB JOURNAL, v. 35, n. 5, MAY 2021. (19/00341-9, 16/00440-9)