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Colony growth of human hematopoietic progenitor cells in the absence of serum is supported by a proteinase inhibitor identified as antileukoproteinase

机译:在没有血清的情况下,人类造血祖细胞的集落生长得到了蛋白酶抑制剂的支持,该蛋白酶抑制剂被称为抗白细胞蛋白酶

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摘要

Serum contains many growth factors and nutrients that stimulate colony formation of hematopoietic progenitor cells (HPC) in semisolid cultures. In the absence of serum, no proliferation of HPCs could be obtained in semisolid medium cultures of partially purified bone marrow cells in the presence of multiple hematopoietic growth factors, insulin, cholesterol, and purified clinical-grade human albumin. This appeared to be due to a suppressive activity induced by monocyte- and T lymphocyte-depleted accessory cells on CD34+ HPCs. Serum-free conditioned medium from the bladder carcinoma cellline 5637 could replace serum to support the growth of HPCs in these cultures. After gel filtration and reverse-phase high-performance liquid chromatography of 5637 supernatants, this activity could be attributed to a 15-kD protein that was further identified by NH2-terminal sequence analysis as the serine proteinase inhibitor antileukoproteinase (ALP). The growth-supportive activity from the 5637 conditioned medium and the (partially) purified fractions could be completely neutralized by a polyclonal rabbit IgG antibody against human ALP (huALP). Similar supportive effects on the growth of HPC could be obtained in the presence of recombinant huALP. We demonstrated that the COOH-terminal domain of ALP containing the proteinase inhibitory activity was responsible for this effect. alpha-1 proteinase inhibitor was capable of similar support of in vitro HPC growth. These results illustrate that proteinase inhibitors play an important role in the in vitro growth of hematopoietic cells by the neutralization of proteinases produced by bone marrow accessory cells. This may be of particular relevance for in vitro expansion of human hematopoietic stem cells in serum-free media.
机译:血清中含有许多生长因子和营养物质,可刺激半固体培养物中的造血祖细胞(HPC)集落形成。在没有血清的情况下,在存在多种造血生长因子,胰岛素,胆固醇和纯化的临床级人白蛋白的情况下,在部分纯化的骨髓细胞的半固体培养基中无法获得HPC的增殖。这似乎是由于单核细胞和T淋巴细胞贫化的辅助细胞对CD34 + HPC诱导的抑制活性。来自膀胱癌细胞系5637的无血清条件培养基可以替代血清,以支持这些培养物中HPC的生长。在对5637个上清液进行凝胶过滤和反相高效液相色谱分析后,此活性可归因于15-kD蛋白,该蛋白通过NH2末端序列分析进一步确定为丝氨酸蛋白酶抑制剂抗白蛋白蛋白酶(ALP)。来自5637条件培养基和(部分)纯化级分的生长支持活性可以被抗人ALP的多克隆兔IgG抗体(huALP)完全中和。在重组huALP的存在下,可以获得对HPC生长的类似支持作用。我们证明了含有蛋白酶抑制活性的ALP的COOH末端域是造成这种效应的原因。 α-1蛋白酶抑制剂能够类似地支持体外HPC生长。这些结果说明蛋白酶抑制剂通过中和由骨髓辅助细胞产生的蛋白酶在造血细胞的体外生长中起重要作用。这对于在无血清培养基中体外扩增人造血干细胞可能具有特殊意义。

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