Cell division orientation must be tightly controlled for the generation of normal tissue architecture. In the skin, asymmetric cell divisions that are driven by oriented mitotic spindles promote both the stratification and differentiation of the embryonic epidermis. While some of the proteins required for spindle orientation have been identified, we do not fully understand how this molecular machinery generates forces on astral microtubules to allow precise control of cell division orientation. In addition, the essential requirement of spindle orientation in embryonic epidermal development has prevented analysis of the function of these divisions in adult skin. Roles for spindle orientation in the morphogenesis of hair follicles, which are highly organized epidermal appendages, have not been addressed. Similarly, whether spindle orientation is required for homeostasis of the adult interfollicular epidermis has not been tested. This is despite long- standing hypotheses that loss of spindle orientation could promote tumorigenesis. Our preliminary studies have identified an unexpected mechanism required for spindle orientation in keratinocytes which we will elucidate in detail in Aim 1. These mechanistic studies allowed us to generate a mutant mouse model in which spindle orientation was randomized in the epidermis, resulting in neonatal lethality. Importantly, disruption of spindle orientation in adult animals caused both severe hair follicle defects and interfollicular hyperproliferation and local invasion. We will use this new genetic model to determine the specific roles for spindle orientation in hair follicle morphogenesis (Aim 2) and adult interfollicular epidermal homeostasis and tumorigenesis (Aim 3). Together, these data will provide a deeper mechanistic understanding of spindle orientation which has essential functions in epidermal, cardiac and neural development as well as the adaptive immune response. In addition this work has direct relevance for both understanding and eventually treating alopecias/hair follicle disorders and skin cancer.

Public Health Relevance

The skin forms an essential barrier that protects us from the environment. The goals of this study are to determine the roles of cell division orientation in promoting skin and hair development, homeostasis and in tumor formation. This work will both test long-standing hypotheses for the role of spindle orientation in suppressing tumor growth as well as contribute to the development of clinical approaches for treating barrier dysfunction in pre-term infants and in burn victims.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR067203-02
Application #
9118867
Study Section
Arthritis, Connective Tissue and Skin Study Section (ACTS)
Program Officer
Baker, Carl
Project Start
2015-09-01
Project End
2020-08-31
Budget Start
2016-09-01
Budget End
2017-08-31
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Duke University
Department
Dermatology
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Muroyama, Andrew; Terwilliger, Michael; Dong, Bushu et al. (2018) Genetically induced microtubule disruption in the mouse intestine impairs intracellular organization and transport. Mol Biol Cell 29:1533-1541
Sumigray, Kaelyn D; Terwilliger, Michael; Lechler, Terry (2018) Morphogenesis and Compartmentalization of the Intestinal Crypt. Dev Cell 45:183-197.e5
Muroyama, Andrew; Lechler, Terry (2017) A transgenic toolkit for visualizing and perturbing microtubules reveals unexpected functions in the epidermis. Elife 6:
Muroyama, Andrew; Lechler, Terry (2017) Microtubule organization, dynamics and functions in differentiated cells. Development 144:3012-3021
Seldin, Lindsey; Muroyama, Andrew; Lechler, Terry (2016) NuMA-microtubule interactions are critical for spindle orientation and the morphogenesis of diverse epidermal structures. Elife 5: