Immune and Gene Therapy Laboratory, Cancer Centre Karolinska, Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
PLoS One. 2013 Jun 24;8(6):e67601. doi: 10.1371/journal.pone.0067601. Print 2013.
Proline/arginine-rich end leucine-rich repeat protein (PRELP) belongs to the small leucine-rich proteoglycan (SLRP) family, normally expressed in extracellular matrix of collagen-rich tissues. We have previously reported on another SLRP, fibromodulin (FMOD) in patients with chronic lymphocytic leukemia (CLL). PRELP is structurally similar to FMOD with adjacent localization on chromosome 1 (1q32.1). As cluster-upregulation of genes may occur in malignancies, the aim of our study was to analyze PRELP expression in CLL. PRELP was expressed (RT-PCR) in all CLL patients (30/30), as well as in some patients with mantle cell lymphoma (3/5), but not in healthy donor leukocytes (0/20) or tumor samples from other hematological malignancies (0/35). PRELP was also detected in CLL cell-lines (4/4) but not in cell-lines from other hematological tumors (0/9). PRELP protein was detected in all CLL samples but not in normal leukocytes. Deglycosylation experiments revealed a CLL-unique 38 kDa core protein, with an intact signal peptide. This 38 kDa protein was, in contrast to the normal 55 kDa size, not detected in serum which, in combination with the uncleaved signal peptide, suggests cellular retention. The unique expression of a 38 kDa PRELP in CLL cells may suggest involvement in the pathobiology of CLL and merits further studies.
脯氨酸/精氨酸丰富的末端亮氨酸丰富的重复蛋白(PRELP)属于小富含亮氨酸的蛋白聚糖(SLRP)家族,通常在富含胶原蛋白的组织的细胞外基质中表达。我们之前曾报道过另一种 SLRP,即纤维调节蛋白(FMOD)在慢性淋巴细胞白血病(CLL)患者中。PRELP 与 FMOD 结构相似,在染色体 1(1q32.1)上的相邻定位。由于簇基因的上调可能发生在恶性肿瘤中,因此我们研究的目的是分析 CLL 中的 PRELP 表达。PRELP 在所有 CLL 患者(30/30)中均有表达(RT-PCR),在一些套细胞淋巴瘤患者(3/5)中也有表达,但在健康供体白细胞(0/20)或其他血液恶性肿瘤的肿瘤样本中(0/35)没有表达。PRELP 也在 CLL 细胞系(4/4)中检测到,但在其他血液肿瘤细胞系(0/9)中没有检测到。在所有 CLL 样本中均检测到 PRELP 蛋白,但在正常白细胞中未检测到。去糖基化实验显示 CLL 独特的 38 kDa 核心蛋白,具有完整的信号肽。与正常的 55 kDa 大小相比,这种 38 kDa 蛋白未在血清中检测到,与未切割的信号肽结合,提示细胞内滞留。CLL 细胞中独特表达的 38 kDa PRELP 可能提示其参与 CLL 的病理生物学,值得进一步研究。