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Active NON-SBIR/STTR RPGS NIH (US)

Functional and therapeutic roles of the Hedgehog signaling in meibomian glands development, renewal and dysfunction

$4.42M USD

Funder NATIONAL EYE INSTITUTE
Recipient Organization Johns Hopkins University
Country United States
Start Date Jul 01, 2024
End Date Jun 30, 2029
Duration 1,825 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10859607
Grant Description

Meibomian gland disease (MGD) is considered the leading cause of dry eye disease, a common multifactorial disease with a global prevalence of 5 to 50% and a major age-related disease of the ocular surface. Meibomian glands (MG) are modified sebaceous glands that line the margin of the eyelid, secrete lipids at the ocular surface,

and participate in increasing the stability of the tear film. MGs are holocrine glands, which implies they are continually renewed since they deliver their secretory product, called meibum, by apoptosis. Thus, regulation of MG stem cells is crucial to ensure the proper function of MGs. With the aging process or disease condition, MGs

can progressively lose their renewal capability and regress to an atrophic state. The pathogenesis of MGD and the mechanisms by which aging affects the renewal process remain largely unknown. Treatment options are currently limited mainly due to the lack of clear therapeutic targets and effective drug delivery strategies targeting

the tissue of MGs. Thus, there is a critical need to understand signaling cascades underlying the renewal process of the MG that can be pharmacologically targeted to treat MGD. Our recent advances, with the aid of an NIH/NEI R21 (EY030661), have led us to discover a novel role of the primary cilium in MG development and maintenance

suggesting a role of HH in the this process. The Hedgehog (HH) pathway plays a fundamental role in tissue development, homeostasis, and repair, including adult stem cell maintenance. To determine the therapeutic potential of targeting the HH pathway to treat MGD, we will investigate its role in MG development, maintenance,

and renewal and trace the cell lineage of HH-responsive cells involved in MG homeostasis. We will target the HH pathway in mice using genetic and pharmacological HH modulators to improve age-related MGD. If successful, the outcome of this work will reveal mechanistic insights into MG renewal and define a novel

paradigm for how to approach novel treatment strategies for MGD.

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Johns Hopkins University

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