Accession Number:



Modeling TSC and LAM Using Patient Derived Induced Pluripotent Stem Cells

Descriptive Note:

Technical Report,30 Sep 2015,29 Sep 2016

Corporate Author:

University of Ottawa Ottawa Canada

Personal Author(s):

Report Date:


Pagination or Media Count:



Tuberous sclerosis complex TSC is a multi-organ genetic disorder with an estimated incidence of one in 6,000 live births due to mutations in either TSC1 or TSC2. About 30 of women with TSC have lymphangioleiomyomatosis LAM, a progressive lung disease characterized by abnormal proliferation of smooth muscle-like cells throughout the lungs, leading to lung destruction and eventual respiratory failure. The cause of the tumor development in various tissues is not well understood, in part due to a lack of human TSC1 or TSC2 deficient human cells to study the biology of the disease and perform drug screens. We have now made TSC2deficient human cells using patient induced pluripotent stem cells iPSCs, lentiviral knockdown, and CRISPRCas9 genome editing in embryonic stem cells ESCs. We have characterized the iPSCs extensively and found that they display abnormal cell size, autophagy regulation, metabolic activity, hyperactive mTOR signaling, and differentiation all characteristics of TSC and LAM cells.

Subject Categories:

Distribution Statement: