Department of Medicine, Duke University, Durham, NC 27710, USA.
Am J Physiol Gastrointest Liver Physiol. 2010 Apr;298(4):G518-24. doi: 10.1152/ajpgi.00431.2009. Epub 2010 Jan 28.
Endogenous trypsin inhibitors are synthesized, stored, and secreted by pancreatic acinar cells. It is believed that they play a protective role in the pancreas by inhibiting trypsin within the cell should trypsinogen become prematurely activated. Rodent trypsin inhibitors are highly homologous to human serine protease inhibitor Kazal-type 1 (SPINK1). The mouse has one pancreatic trypsin inhibitor known as SPINK3, and the rat has two trypsin inhibitors commonly known as pancreatic secretory trypsin inhibitors I and II (PSTI-I and -II). Rat PSTI-I is a 61-amino acid protein that shares 65% sequence identity with mouse SPINK3. It was recently demonstrated that mice with genetic deletion of the Spink3 gene (Spink3(-/-)) do not survive beyond 15 days and lack normal pancreata because of pancreatic autophagy. We have shown that targeted transgenic expression of the rat Psti1 gene to acinar cells in mice [TgN(Psti1)] protects mice against caerulein-induced pancreatitis. To determine whether the autophagic phenotype and lethality in Spink3(-/-) mice were due to lack of pancreatic trypsin inhibitor, we conducted breeding studies with Spink3(+/-) heterozygous mice and TgN(Psti1) mice. We observed that, whereas Spink3(+/+), Spink3(+/-), and Spink3(-/-)/TgN(Psti1) mice had similar survival rates, no Spink3(-/-) mice survived longer than 1 wk. The level of expression of SPINK3 protein in acini was reduced in heterozygote mice compared with wild-type mice. Furthermore, endogenous trypsin inhibitor capacity was reduced in the pancreas of heterozygote mice compared with wild-type or knockout mice rescued with the rat Psti1 gene. Surprisingly, the lesser amount of SPINK3 present in the pancreata of heterozygote mice did not predispose animals to increased susceptibility to caerulein-induced acute pancreatitis. We propose that a threshold level of expression is sufficient to protect against pancreatitis.
内源性胰蛋白酶抑制剂由胰腺腺泡细胞合成、储存和分泌。人们认为,它们在胰腺中发挥保护作用,通过抑制细胞内的胰蛋白酶,防止胰蛋白酶原过早激活。啮齿动物的胰蛋白酶抑制剂与人丝氨酸蛋白酶抑制剂 Kazal 型 1(SPINK1)高度同源。小鼠有一种称为 SPINK3 的胰腺胰蛋白酶抑制剂,大鼠有两种通常称为胰腺分泌性胰蛋白酶抑制剂 I 和 II(PSTI-I 和 -II)的胰蛋白酶抑制剂。大鼠 PSTI-I 是一种 61 个氨基酸的蛋白质,与小鼠 SPINK3 有 65%的序列同一性。最近的研究表明,基因敲除 Spink3 基因(Spink3(-/-))的小鼠在 15 天内不能存活,并且由于胰腺自噬而缺乏正常的胰腺。我们已经证明,靶向转基因表达大鼠 Psti1 基因到小鼠的腺泡细胞[TgN(Psti1)]可保护小鼠免受 caerulein 诱导的胰腺炎。为了确定 Spink3(-/-)小鼠中的自噬表型和致死性是否是由于缺乏胰腺胰蛋白酶抑制剂引起的,我们用 Spink3(+/-)杂合子小鼠和 TgN(Psti1)小鼠进行了繁殖研究。我们观察到,尽管 Spink3(+/+)、Spink3(+/-)和 Spink3(-/-)/TgN(Psti1)小鼠的存活率相似,但没有 Spink3(-/-)小鼠存活超过 1 周。与野生型小鼠相比,杂合子小鼠腺泡中的 SPINK3 蛋白表达水平降低。此外,与野生型或用大鼠 Psti1 基因拯救的敲除小鼠相比,杂合子小鼠胰腺中的内源性胰蛋白酶抑制剂能力降低。令人惊讶的是,杂合子小鼠胰腺中存在的 SPINK3 量较少并没有使动物更容易受到 caerulein 诱导的急性胰腺炎的影响。我们提出,表达的阈值足以保护免受胰腺炎。