Cyclic growth of dermal papilla and regeneration of follicular mesenchymal components during feather cycling

Author:

Wu Ping1ORCID,Jiang Ting-Xin1ORCID,Lei Mingxing23ORCID,Chen Chih-Kuan14ORCID,Hsieh Li Shu-Man156ORCID,Widelitz Randall B.1ORCID,Chuong Cheng-Ming1ORCID

Affiliation:

1. Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA

2. 111 Project Laboratory of Biomechanics and Tissue Repair, College of Bioengineering, Chongqing University, Chongqing 400044, China

3. Integrative Stem Cell Center, China Medical University Hospital, China Medical University, Taichung 40402, Taiwan

4. The IEGG and Animal Biotechnology Center, National Chung Hsing University, Taichung 402, Taiwan

5. Center for Craniofacial Molecular Biology, Ostrow School of Dentistry, University of Southern California, Los Angeles, CA 90033, USA

6. Department of Biochemistry, National Defense Medical Center, Taipei 114, Taiwan

Abstract

ABSTRACT How dermis maintains tissue homeostasis in cyclic growth and wounding is a fundamental unsolved question. Here, we study how dermal components of feather follicles undergo physiological (molting) and plucking injury-induced regeneration in chickens. Proliferation analyses reveal quiescent, transient-amplifying (TA) and long-term label-retaining dermal cell (LRDC) states. During the growth phase, LRDCs are activated to make new dermal components with distinct cellular flows. Dermal TA cells, enriched in the proximal follicle, generate both peripheral pulp, which extends distally to expand the epithelial-mesenchymal interactive interface for barb patterning, and central pulp, which provides nutrition. Entering the resting phase, LRDCs, accompanying collar bulge epidermal label-retaining cells, descend to the apical dermal papilla. In the next cycle, these apical dermal papilla LRDCs are re-activated to become new pulp progenitor TA cells. In the growth phase, lower dermal sheath can generate dermal papilla and pulp. Transcriptome analyses identify marker genes and highlight molecular signaling associated with dermal specification. We compare the cyclic topological changes with those of the hair follicle, a convergently evolved follicle configuration. This work presents a model for analyzing homeostasis and tissue remodeling of mesenchymal progenitors.

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

University of Southern California

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Chongqing University

National Chung Hsing University

Ministry of Science and Technology, Taiwan

Ministry of National Defense of Taiwan

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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