Yaar M, Eller M S, Bhawan J, Harkness D D, DiBenedetto P J, Gilchrest B A
Department of Dermatology, Boston University School of Medicine, Massachusetts 02118, USA.
Exp Cell Res. 1995 Apr;217(2):217-26. doi: 10.1006/excr.1995.1081.
The small proline-rich protein 1 (SPRR1) gene encodes a precursor of the keratinocyte cornified envelope. To understand SPRR1 regulation we investigated its expression and modulation in keratinocytes in vivo and in vitro. SPRR1 was strongly expressed in suprabasal layers of the epidermis in newborn skin but only weakly expressed in adult skin. Both in vivo and in vitro, SPRR1 was not expressed in undifferentiated cells of basal or squamous carcinomas. However, within the same tumors and in premalignant lesions of squamous cell origin, cells with histologic evidence of differentiation showed a relative increase in SPRR1 transcript level. Within 24 h physiologic doses of uv irradiation induced SPRR1 mRNA in vivo. To investigate the possibility that SPRR1 expression is regulated by uv-induced cytokines, keratinocytes were stimulated with interleukin-1 (IL-1) and interleukin-3 (IL-3). Both significantly induced SPRR1 mRNA, while TGF-beta, known to lower IL-1 receptor in keratinocytes, down-regulated it. Moreover, proximity to inflammatory cells in vivo was associated with SPRR1 induction in anaplastic tumor cells. Our data suggest that SPRR1 is induced early in differentiation of normal keratinocytes but is not expressed in anaplastic cells of keratinocyte origin. Further, its regulation in skin appears to be modulated at least in part through cytokine release.
富含脯氨酸的小分子蛋白1(SPRR1)基因编码角质形成细胞角质化包膜的前体。为了解SPRR1的调控机制,我们研究了其在体内和体外角质形成细胞中的表达及调节情况。SPRR1在新生皮肤表皮的基底上层强烈表达,但在成人皮肤中表达较弱。在体内和体外,基底癌或鳞状细胞癌的未分化细胞中均未检测到SPRR1的表达。然而,在同一肿瘤以及鳞状细胞起源的癌前病变中,具有组织学分化证据的细胞显示出SPRR1转录水平相对升高。在24小时内,生理剂量的紫外线照射可在体内诱导SPRR1 mRNA表达。为研究SPRR1表达是否受紫外线诱导的细胞因子调控,我们用白细胞介素-1(IL-1)和白细胞介素-3(IL-3)刺激角质形成细胞。二者均能显著诱导SPRR1 mRNA表达,而已知可降低角质形成细胞中IL-1受体水平的转化生长因子-β(TGF-β)则下调其表达。此外,在体内,间变肿瘤细胞中SPRR1的诱导表达与炎症细胞的接近有关。我们的数据表明,SPRR1在正常角质形成细胞分化早期被诱导表达,但在角质形成细胞来源的间变细胞中不表达。此外,其在皮肤中的调控似乎至少部分受细胞因子释放的调节。