Similarly potent action of 1,25-dihydroxyvitamin D3 and its analogues, tacalcitol, calcipotriol, and maxacalcitol on normal human keratinocyte proliferation and differentiation

2003 ◽  
Vol 31 (1) ◽  
pp. 21-28 ◽  
Author(s):  
Hidetoshi Takahashi ◽  
Masaki Ibe ◽  
Motoshi Kinouchi ◽  
Akemi Ishida-Yamamoto ◽  
Yoshio Hashimoto ◽  
...  
1998 ◽  
Vol 17 (2) ◽  
pp. 108-114 ◽  
Author(s):  
Teruaki Kobayashi ◽  
Hidenobu Okumura ◽  
Koji Hashimoto ◽  
Hideo Asada ◽  
Shigeki Inui ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Bénédicte Oulès ◽  
Christina Philippeos ◽  
Joe Segal ◽  
Matthieu Tihy ◽  
Matteo Vietri Rudan ◽  
...  

Abstract Although acne is the most common human inflammatory skin disease, its pathogenic mechanisms remain incompletely understood. Here we show that GATA6, which is expressed in the upper pilosebaceous unit of normal human skin, is down-regulated in acne. GATA6 controls keratinocyte proliferation and differentiation to prevent hyperkeratinisation of the infundibulum, which is the primary pathological event in acne. When overexpressed in immortalised human sebocytes, GATA6 triggers a junctional zone and sebaceous differentiation program whilst limiting lipid production and cell proliferation. It modulates the immunological repertoire of sebocytes, notably by upregulating PD-L1 and IL10. GATA6 expression contributes to the therapeutic effect of retinoic acid, the main treatment for acne. In a human sebaceous organoid model GATA6-mediated down-regulation of the infundibular differentiation program is mediated by induction of TGFβ signalling. We conclude that GATA6 is involved in regulation of the upper pilosebaceous unit and may be an actionable target in the treatment of acne.


Blood ◽  
1996 ◽  
Vol 87 (7) ◽  
pp. 2693-2701 ◽  
Author(s):  
K Nakamura ◽  
T Takahashi ◽  
Y Sasaki ◽  
R Tsuyuoka ◽  
Y Okuno ◽  
...  

Although it is well established that the addition of 1,25- dihydroxyvitamin D3 (D3) to the culture of normal human granulocyte/macrophage progenitors induces monocyte/macrophage (Mo/M phi) colonies, the target cells of D3 in the Mo/M phi differentiation have not been identified. We examined whether neutrophilic promyelocytes are the target cells. As a source of the promyelocyte fraction, we used colonies after 5 days of culture (5-day colonies) of colony-forming unit-granulocyte. The culture contained granulocyte colony-stimulating factor (G-CSF) as the growth factor and generated only neutrophilic colonies. The promyelocytic nature of the 5-day colonies was confirmed morphologically, cytochemically, and ultrastructurally. After morphological evaluation on part of the individual colonies, they were transferred into new semisolid cultures with or without D3 (10(-7) mol/L) in the presence of G-CSF, then incubated for the subsequent 7 days. With D3, the colonies were loose, and all the constituent cells were morphologically small macrophages, which were positive for alpha-naphthyl butyrate (alpha NB) esterase, strongly positive for CD14 antigen, and plastic-adherent. While without D3, the colonies were rather compact, and all the constituent cells were morphologically mature neutrophils, which were positive for naphthol ASD-chloroacetate esterase and weakly positive for CD14 antigen. Secondary culture of the 8- or 10-day colonies with D3 induced a lower number of alpha NB-positive cells, in proportion to the percentage of promyelocytes at the time of transfer in each colony. Four days of secondary culture with D3 was sufficient to induce alpha NB-positive cells. G-CSF was not an essential factor to induce alpha NB- positive cells. These findings indicate that D3 differentiates normal human neutrophilic promyelocytes into the Mo/M phi lineage in vitro.


1985 ◽  
Vol 127 (2) ◽  
pp. 596-603 ◽  
Author(s):  
H. Phillip Koeffler ◽  
Helmut Reichel ◽  
June E. Bishop ◽  
Anthony W. Norman

Bone ◽  
1987 ◽  
Vol 8 (4) ◽  
pp. 264
Author(s):  
U. Berger ◽  
P. Wilson ◽  
K. Colston ◽  
R.C. Coombes ◽  
J.W. Pike ◽  
...  

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