Mechanical forces powerfully modulate stem cell fate. Despite the emerging importance of these forces in stem cell differentiation, the molecular mechanisms by which mechanical cues direct cell fate remain unknown. We propose that the stretch-activated ion channels (SACs) transduce mechanical information sensed at the plasma membrane to downstream signaling molecules that control cell fate. In this revised application we will test this hypothesis in light of new preliminary data from our group demonstrating that the recently-identified SAC Piezo1 underlies mechanotransduction currents in human neural stem/progenitor cells and influences neuronal-glial lineage choice.
In Aim 1 we will directly test the hypothesis that Piezo1 links mechanical signals to downstream transcription factor activity and mechanosensitive lineage specification.
In Aim 2 we will determine whether Piezo1 activity is involved in lineage specification in vivo. Together, the two Aims will establish Piezo1 as a ke signaling molecule in mechanoregulation of human neural stem/progenitor cell fate. In summary, this proposal brings together our expertise in ion channel biophysics, mechanics, biomaterials and stem cell biology to uncover a new molecular player with implications for both, basic stem cell biology and future developments in regenerative medicine.

Public Health Relevance

Human neural stem/progenitor cells (hNSPCs) are capable of generating the three main cell-types found in the brain - neurons, astrocytes and oligodendrocytes. Hence they hold great promise for neural repair after injury or disease (e.g. spinal cord injury, Alzheimer's disease, Parkinson's disease etc.). The goal of this proposal is t understand the mechanisms by which mechanical signals encountered by hNSPCs in vitro and in vivo influence their fate. Successful completion of the project will bring new insights to neurl stem cell biology which will potentially lead to improvements in neural repair strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21NS085628-02
Application #
8997126
Study Section
Special Emphasis Panel (BNVT)
Program Officer
Lavaute, Timothy M
Project Start
2015-02-01
Project End
2017-01-31
Budget Start
2016-02-01
Budget End
2017-01-31
Support Year
2
Fiscal Year
2016
Total Cost
$193,125
Indirect Cost
$68,125
Name
University of California Irvine
Department
Physiology
Type
Schools of Medicine
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92617
Nourse, Jamison L; Pathak, Medha M (2017) How cells channel their stress: Interplay between Piezo1 and the cytoskeleton. Semin Cell Dev Biol 71:3-12
Phan, Long; Kautz, Rylan; Arulmoli, Janahan et al. (2016) Reflectin as a Material for Neural Stem Cell Growth. ACS Appl Mater Interfaces 8:278-84
Pathak, Medha M; Tran, Truc; Hong, Liang et al. (2016) The Hv1 proton channel responds to mechanical stimuli. J Gen Physiol 148:405-418