CHANGES IN GROWTH AND PANCREATIC MESSENGER-RNA CONCENTRATIONS DURING POSTNATAL-DEVELOPMENT OF RAT PANCREAS

被引：12

作者：

IOVANNA, JL

DUSETTI, N

CADENAS, B

CALVO, EL

机构：

[1] Departamento de Fisiología, Universidad de Beunos Aires, Buenos Aires

来源：

PANCREAS | 1990年 / 5卷 / 04期

关键词：

Actin; Amylase; Chymo-trypsinogen; Pancreas development; Pancreatic mRNAs; Proinsulin;

D O I：

10.1097/00006676-199007000-00008

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

Changes in pancreatic growth and in mRNA concentrations in rat pancreas were monitored by dot-blot hybridization with cloned cDNAs of rat amylase, chymotrypsinogen B, proinsulin I, and actin during the pre-and postnatal period in the rat. Wistar rats were killed at the 18th day of gestation and at the 1st, 10th, 20th, 35th, and 87th day of postnatal life. It was concluded from the ratio of pancreatic weight/body weight that pancreatic growth preceded body growth. Pancreatic protein and total RNA concentration increased 2.9 times during the period studied. All studied mRNAs increased in concentration during the postnatal development period. Messenger RNA for chymotrypsinogen B and proinsulin I exhibited a significant increase after birth, decreased by the 10th day of life, and increased thereafter. For amylase mRNA, no significant changes were observed around birth, a progressive increase occurring thereafter up to the 87th day of life. The mRNA for actin showed a progressive increase between the 18th day of gestation and the 20th postnatal day, after which it remained stable. We concluded that each mRNA showed a singular profile of increase during postnatal development. © 1990 Raven Press Ltd., New York.

引用

页码：421 / 426

页数：6

共 28 条

[11]

Volkin E., Cohn W., Estimation of nucleic acids, Methods Biochem Anal, 1, pp. 287-303, (1954)

[12]

Lowry O., Rosebrough N., Farr A., Randall R., Protein measurement with the folin phenol reagent, J Biol Chem, 193, pp. 265-275, (1951)

[13]

Barnard E., Biological function of pancreatic ribonuclease, Nature (Lond), 221, pp. 340-344, (1969)

[14]

Chirgwin J., Przybyla A., Mac Donald R., Rutter W., Isolation of biologically active ribonucleic acid from sources enriched in ribonucleases, Biochemistry, 19, pp. 5294-5299, (1979)

[15]

Bailey J., Davidson N., Methylmercury as a reversible denaturing agent for agarose gel electrophoresis, Anal Biochem, 70, pp. 75-85, (1976)

[16]

Uchiyama Y., Watanabe M., A morphometric study of developing pancreatic acinar cells of rats during prenatal life, Cell Tissue Res, 237, pp. 117-122, (1984)

[17]

Uchiyama Y., Watanabe M., Morphometric and fine-structural studies of rat pancreatic cells during early postnatal life, Cell Tissue Res, 237, pp. 123-129, (1984)

[18]

Rutter W., Przybyla A., Mac Donald R., Harding J., Chirgwin J., Pictet R., Pancreas development: An analysis of differentiation at the transcriptional level, Cell Differentiation and Neoplasia, pp. 487-508, (1978)

[19]

Solomon T., Grossman M., Effect of atropine and vagotomy on response of transplanted pancreas, Am J Physiol, 246, pp. 186-190, (1979)

[20]

Johnson L., The trophic action of gastrointestinal hormones, Gastroenterology, 70, pp. 278-288, (1976)

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