Taming psoriatic keratinocytes—PTHs' uses go up another notch
✍ Scribed by James F. Whitfield
- Book ID
- 102300291
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 190 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The native parathyroid hormone (PTH) and several of its N‐terminal adenylyl cyclase‐activating fragments and their analogs have become the star stimulators of bone growth for treating osteoporosis, accelerating fracture healing, and strengthening the anchorage of prosthetic bone implants and one of them (Lilly's Forteo™—recombinant hPTH‐(1‐34) has recently arrived in the clinic. But something entirely different has been lurking in the background—the ability of the adenylyl cyclase stimulating hPTH‐(1‐34) to calm hyperproliferating keratinocytes and reduce psoriatic lesions. By contrast PTH‐(7‐34) which cannot stimulate adenylyl cyclase actually stimulates keratinocyte proliferation. Normal keratinocytes make PTHrP after they lift off the basal lamina and have stopped cycling. But they have an unconventional PTH/PTHrP receptorr which is not coupled to adenylyl cyclase. Psoriatic keratinocytes do not make PTHrP and have only a broken‐down, proliferation‐limiting terminal differentiation‐driving Notch–Notch ligand mechanism. Putting these and other facts together produces a possible picture of an exogenously applied adenylyl cyclase‐activating PTH pinch hitting for the missing PTHrP and restoring normal keratinocyte proliferative activity epidermal structure by stimulating dermal fibroblasts which do have the conventional adenylyl cyclasse‐linked PTHR1 and in response directly or indirectly restore the overlying basal keratinocytes' Notch–Notch ligand terminal differentiation‐driving mechanism and consequently a normal epidermal structure. © 2004 Wiley‐Liss, Inc.