Literature DB >> 11984874

HOXB4 homeodomain protein is expressed in developing epidermis and skin disorders and modulates keratinocyte proliferation.

László G Kömüves1, Elias Michael, Jeffrey M Arbeit, Xiao-Kui Ma, Angela Kwong, Eric Stelnicki, Sophia Rozenfeld, M Morimune, Qian-Chun Yu, Corey Largman.   

Abstract

The HOX homeodomain proteins are fundamental regulators of organ and tissue development, where they are thought to function as transcription factors, and HOX gene expression has been associated with numerous types of cancers. Previous studies have demonstrated that enforced expression of the HOXB4 protein transforms cultured fibroblasts and leads to a selective expansion of the hematopoietic stem cell pool, suggesting that this protein might play a role in cellular proliferation. In support of this concept, we now show that enforced expression of HOXB4 in human neonatal keratinocytes results in increased cellular proliferation and colony formation as well as decreased expression of the alpha-2-integrin and CD44 cell surface adhesion molecules. We previously have reported HOXB4 gene expression in the basal and suprabasal layers of developing human skin and now show extensive HOXB4 mRNA in psoriatic skin and basal cell carcinoma. In fetal human skin HOXB4 protein expression was both nuclear and cytoplasmic within epidermal basal cells and in hair follicle inner and outer root sheath cells, whereas strong nuclear signals were observed in the bulge region. In adult skin, HOXB4 protein expression was both nuclear and cytoplasmic, but was predominantly localized to the intermediate and differentiated cell layers. In contrast to the striking gradient patterns of HOX gene and protein expression previously described in developing spinal cord and limb, HOXB4 protein was uniformly detected in all regions of the fetal and adult skin. Although little HOXB4 signal localized to proliferative cell layers, as marked by proliferating cell nuclear antigen (PCNA) staining, in normal adult epidermis, nuclear HOXB4 protein expression substantially overlapped with PCNA-positive cell in a series of samples of hyperproliferative skin. Taken together, these data suggest that nuclear HOXB4 protein may play a role in the regulation of cellular proliferation/adhesion in developing fetal human epidermis and in hyperproliferation conditions, including cancers, in adult epidermis. Published 2002 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11984874     DOI: 10.1002/dvdy.10085

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  9 in total

1.  Homeobox genes, fetal wound healing, and skin regional specificity.

Authors:  Cheng-Ming Chuong
Journal:  J Invest Dermatol       Date:  2003-01       Impact factor: 8.551

Review 2.  Tissue engineering of replacement skin: the crossroads of biomaterials, wound healing, embryonic development, stem cells and regeneration.

Authors:  Anthony D Metcalfe; Mark W J Ferguson
Journal:  J R Soc Interface       Date:  2007-06-22       Impact factor: 4.118

Review 3.  Hox genes and their candidate downstream targets in the developing central nervous system.

Authors:  Z N Akin; A J Nazarali
Journal:  Cell Mol Neurobiol       Date:  2005-06       Impact factor: 5.046

Review 4.  Hox in hair growth and development.

Authors:  Alexander Awgulewitsch
Journal:  Naturwissenschaften       Date:  2003-04-26

5.  MicroRNA-126 regulates HOXA9 by binding to the homeobox.

Authors:  Wei-Fang Shen; Yu-Long Hu; Lalita Uttarwar; Emmanuelle Passegue; Corey Largman
Journal:  Mol Cell Biol       Date:  2008-05-12       Impact factor: 4.272

6.  C/EBPδ gene targets in human keratinocytes.

Authors:  Serena Borrelli; Daniele Fanoni; Diletta Dolfini; Daniela Alotto; Maria Ravo; Olì Maria Victoria Grober; Alessandro Weisz; Carlotta Castagnoli; Emilio Berti; M Alessandra Vigano; Roberto Mantovani
Journal:  PLoS One       Date:  2010-11-02       Impact factor: 3.240

7.  A review of fetal scarless healing.

Authors:  K J Rolfe; A O Grobbelaar
Journal:  ISRN Dermatol       Date:  2012-05-17

8.  Accelerated closure of skin wounds in mice deficient in the homeobox gene Msx2.

Authors:  Jennifer Yeh; Lydia M Green; Ting-Xin Jiang; Maksim Plikus; Eunice Huang; Richard N Chang; Michael W Hughes; Cheng-Ming Chuong; Tai-Lan Tuan
Journal:  Wound Repair Regen       Date:  2009 Sep-Oct       Impact factor: 3.401

Review 9.  HOX Protein Activity Regulation by Cellular Localization.

Authors:  Laure Bridoux; Françoise Gofflot; René Rezsohazy
Journal:  J Dev Biol       Date:  2021-12-07
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.