IL-1 alpha 蛋白, Mouse

IL-1 alpha is a ubiquitous and pivotal pro-inflammatory cytokine. IL-1 alpha is produced by monocytes and macrophages as a proprotein, which is proteolytically processed and released in response to cell injury, and thus induces apoptosis. IL-1 alpha plays an important role in inflammation and bridges the innate and adaptive immune systems. IL-1 alpha mediates the activation of NF-kappa-B and the three MAPK pathways p38, p42/p44 and JNK pathways^[1][2]. IL-1 alpha protein, Mouse is a recombinant protein consisting of 156 amino acids (S115-A270) and is produced by E. coli.

IL-1 α（白细胞介素 1 α）是 IL-1 的主要激动剂。特别是IL-1α存在于所有间充质细胞中，富含IL-1α的细胞构成具有屏障功能的组织，如皮肤中的角质形成细胞、肺中的2型上皮细胞、整个胃肠道的上皮、内皮细胞血管中和大脑中的星形胶质细胞^[1]。IL-1α (ProIL-1α) 的前体由 Ca²⁺ 依赖性蛋白酶钙蛋白酶（包括 caspase-1）加工成成熟的 17 kDa 形式和 16 kDa N 端裂解产物– IL-1α 的前体，也称为 IL-1α N 末端肽 (IL-1NTP)。潜在形式的钙蛋白酶在炎症条件下的细胞中被激活，尤其是在细胞质膜完整性丧失（坏死过程中发生）时。pro-IL-1α 和成熟的 IL-1α 与 IL-1R 结合并诱导 IL-6 和 TNF^[5] 的分泌。IL-1α 充当“警报器”和组织炎症的原动机^[1]。IL-1 α 通过 Myd88 激活启动并最终导致 NF-κB 诱导炎症基因转录的途径引发炎症^[2]。IL-1 α 抑制前脂肪细胞分化和脂质积累^[3]。IL-1 α 诱导细胞凋亡并抑制成骨细胞分化^[4]。

IL-1 alpha (0.5, 1, 2.5, 5, 10 ng/mL; 5 days) significantly reduces the cell viability in MC3T3-E1 cells^[4].
IL-1 alpha (0.5, 1, 2.5, 5, 10 ng/mL 24 h) decreases the ALP and caspase-3 activity in MC3T3-E1 cells, increases the expression of Bax and caspase-3 mRNA and protein level in a dose-dependent manner, decreases the mRNA expression and the protein levels of Runx2, ALP, OSX and OCN; induces apoptosis^[4].

IL-1 alpha (10 µg/kg; i.p.) significantly increases the TG (triglyceride) level at 12 h in serum in C57BL/6J male mice^[3].
IL-1 alpha (1, 10, 100 ng/mL; 8 days) inhibits differentiation of preadipocytes and lipid accumulation in a dose-dependent manner in 3T3-L1 cells^[3].

1. The ED₅₀ is <2 pg/mL as measured by murine D10S cells, corresponding to a specific activity of >5.0 × 10⁸ units/mg.
2. Measured in a proliferation assay using CTLL-2 Mouse T lymphocytes cell. The ED₅₀ for this effect is 0.5597 pg/mL, corresponding to a specific activity is 1.787×10⁹ units/mg.

• 
  Measured in a proliferation assay using CTLL-2 Mouse T lymphocytes cell. The ED₅₀ for this effect is 0.5597pg/mL, corresponding to a specific activity is 1.787×10⁹ units/mg.

Mouse

E. coli

Tag Free

P01582 (S115-S270)

16175  [NCBI]

SAPYTYQSDLRYKLMKLVRQKFVMNDSLNQTIYQDVDKHYLSTTWLNDLQQEVKFDMYAYSSGGDDSKYPVTLKISDSQLFVSAQGEDQPVLLKELPETPKLITGSETDLIFFWKSINSKNYFTSAAYPELFIATKEQSRVHLARGLPSMTDFQIS

Approximately 17 kDa

• 
  Greater than 95% as determined by reducing SDS-PAGE.

无菌粉末.

Lyophilized after extensive dialysis against PBS, pH 7.4 or 50 mM Tris-HCl, 200 mM NaCl, pH 8.0.

<1 EU/μg, determined by LAL method.

It is not recommended to reconstitute to a concentration less than 100 μg/mL in ddH₂O. For long term storage it is recommended to add a carrier protein (0.1% BSA, 5% HSA, 10% FBS or 5% Trehalose).

Stored at -20°C for 2 years. After reconstitution, it is stable at 4°C for 1 week or -20°C for longer (with carrier protein). It is recommended to freeze aliquots at -20°C or -80°C for extended storage.

Room temperature in continental US; may vary elsewhere.

• [1]. Cavalli G, et al. Interleukin 1α: a comprehensive review on the role of IL-1α in the pathogenesis and treatment of autoimmune and inflammatory diseases. Autoimmun Rev. 2021 Mar;20(3):102763.  [Content Brief]

  [2]. Wu T, et al. Involvement of p38 and p42/44 MAP kinases and protein kinase C in the interferon-gamma and interleukin-1alpha-induced phosphorylation of 85-kDa cytosolic phospholipase A(2) in primary human bronchial epithelial cells. Cytokine. 2004 Jan 7;25(1):11-20.  [Content Brief]

  [3]. Um JY, et al. Functional polymorphism of IL-1 alpha and its potential role in obesity in humans and mice. PLoS One. 2011;6(12):e29524.  [Content Brief]

  [4]. Guo C, et al. IL-1α induces apoptosis and inhibits the osteoblast differentiation of MC3T3-E1 cells through the JNK and p38 MAPK pathways. Int J Mol Med. 2016 Jul;38(1):319-27.  [Content Brief]

  [5]. Malik A,et al. Function and regulation of IL-1α in inflammatory diseases and cancer. Immunol Rev. 2018 Jan;281(1):124-137.  [Content Brief]