Abstract
CD44, a cell surface proteoglycan, is involved in many biological events. CD44 transcripts undergo complex alternative splicing, resulting in many functionally distinct isoforms. To date, however, the nature of these isoforms in human epidermis has not been adequately determined. In this study, we isolated all CD44 transcripts from normal human epidermis, and studied how their expressions are regulated. By RT-PCR, we found that a number of different CD44 transcripts were expressed in human epidermis, and we obtained all these transcripts from DNA bands in agarose and acrylamide gels by cloning. Detailed sequence analysis revealed 18 CD44 transcripts, 3 of which were novel. Next, we examined effects of 10 different agents on the expression of CD44 transcripts in cultured human keratinocytes, and found that several agents, particularly epidermal growth factor, hydrogen peroxide, phorbol 12-myristate 13-acetate, retinoic acid, calcium and fetal calf serum differently regulated their expressions in various patterns. Furthermore, normal and malignant keratinocytes were found to produce different CD44 transcripts upon serum stimulation and subsequent starvation, suggesting that specific CD44 isoforms are involved in tumorigenesis via different CD44-mediated biological pathways.
Highlights
CD44 is a cell surface proteoglycan implicated in multiple cell functions, including adhesion, migration, activation, recirculation and homing of lymphocytes, hematopoiesis, tight-junction assembly and tumor metastasis [1,2,3,4]
We investigated the effect of various agents on the expression of CD44 transcript variants in cultured human keratinocytes, in order to shed more light on specific biological pathways mediated by particular CD44 isoforms in human skin
The results revealed that human epidermis has more CD44 diversity than dermis
Summary
CD44 is a cell surface proteoglycan implicated in multiple cell functions, including adhesion, migration, activation, recirculation and homing of lymphocytes, hematopoiesis, tight-junction assembly and tumor metastasis [1,2,3,4]. Recent studies suggested that CD44 is a cancer stem cell marker [5,6]. CD44 is recognized as the principal receptor for hyaluronic acid (HA) [7] and CD44-HA interactions have been demonstrated to affect many physiological and disease processes including promoting keratinocyte activity, improving abnormal epidermal function and melanoma and prostate cancer development [8,9,10,11].
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