Goldstein D J, Levy R, Yu P L, Harris H
Biochem Genet. 1985 Feb;23(1-2):155-67. doi: 10.1007/BF00499120.
Quantitative alkaline phosphatase (ALP; EC 3.1.3.1) expression varies among various tissues and among inbred mouse strains. There is about a 20-fold difference in ALP activity in lungs from CBA/J and C57L/J inbred strains and this difference is inherited additively with a heritability of 0.84. Studies of thermostability at 56 and 65 degrees C and sensitivity toward inhibitors (L-phenylalanine, L-homoarginine, L-phenylalanylglycylglycine, and levamisole) do not demonstrate differences in the ALP from lungs or liver of the CBA/J and C57L/J strains. The ALP activity in intestine expressed by the intestinal locus varies over 100-fold between A/J and DBA/1J strains. Further studies of the mechanisms resulting in this difference in ALP activity should help elucidate the mechanisms for aberrant expression of ALP in malignancy and for manipulation of low ALP activity in hypophosphatasia.
定量碱性磷酸酶(ALP;EC 3.1.3.1)的表达在不同组织以及近交系小鼠品系之间存在差异。CBA/J和C57L/J近交系小鼠肺组织中的ALP活性大约相差20倍,且这种差异以加性方式遗传,遗传力为0.84。对56℃和65℃时热稳定性以及对抑制剂(L-苯丙氨酸、L-高精氨酸、L-苯丙氨酰甘氨酰甘氨酸和左旋咪唑)敏感性的研究未显示CBA/J和C57L/J品系肺组织或肝脏中的ALP存在差异。由肠道位点表达的肠道碱性磷酸酶活性在A/J和DBA/1J品系之间相差超过100倍。对导致这种碱性磷酸酶活性差异的机制进行进一步研究,应有助于阐明恶性肿瘤中碱性磷酸酶异常表达的机制以及低磷酸酯酶症中低碱性磷酸酶活性的调控机制。