Abstract

Little is known about the energetics of growing hair follicles, particularly in the mitochondrially abundant bulb. Here, mitochondrial and oxidative metabolism was visualized by multiphoton and light sheet microscopy in cultured bovine hair follicles and plucked human hairs. Mitochondrial membrane potential (ΔΨ), cell viability, reactive oxygen species (ROS), and secretory granules were assessed with parameter-indicating fluorophores. In growing follicles, lower bulb epithelial cells had high viability, and mitochondria were polarized. Most epithelially generated ROS co-localized with polarized mitochondria. As the imaging plane captured more central and distal cells, ΔΨ disappeared abruptly at a transition to a nonfluorescent core continuous with the hair shaft. Approaching the transition, ΔΨ and ROS increased, and secretory granules disappeared. ROS and ΔΨ were strongest in a circumferential paraxial ring at putative sites for formation of the outer cortex/cuticle of the hair shaft. By contrast, polarized mitochondria in dermal papillar fibroblasts produced minimal ROS. Plucked hairs showed a similar abrupt transition of degranulation/depolarization near sites of keratin deposition, as well as an ROS-generating paraxial ring of fire. Hair movement out of the follicle appeared to occur independently of follicular bulb bioenergetics by a tractor mechanism involving the inner and outer root sheaths.

Highlights

  • On a human scalp, more than 90% of hairs are in the growing or anagen phase (Stenn and Paus, 2001)

  • Mitochondria are important in follicle morphogenesis, because keratinocyte mitochondrial DNA depletion decreases hair follicle density, increases apoptosis, and reduces proliferation

  • A representative follicle prepared for histologic study showed that bulb dermal and epidermal cells were intact and surrounded by a dermal sheath (Figure 1b)

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Summary

Introduction

More than 90% of hairs are in the growing or anagen phase (Stenn and Paus, 2001). Extension of the hair shaft is powered by a poorly understood process of cell proliferation, reshaping, and migration with narrowing of the surrounding inner root sheath, as well as deposition and hardening of keratin (Bornschlogl et al, 2016; Chapman and Gemmell, 1971; Langbein and Schweizer, 2005; Orwin and Woods, 1982; Parry et al, 2007; Plowman et al, 2015; Rafik et al, 2006; Rogers, 1964). Stimulation of mitochondrial function with thyroid hormones prolongs anagen, increases follicular heat production, stimulates hair follicle keratinocyte proliferation, and modifies intrafollicular keratin expression (Kloepper et al, 2015; Van Beek et al, 2008; Vidali et al, 2014, 2016)

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