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钙缺乏、胶原酶和机械分散对成年大鼠心肌细胞超微结构的影响。

Effects of Ca2+ deficiency, collagenase, and mechanical dispersion on the ultrastructure of cardiac myocytes of adult rats.

作者信息

Flegler-Balon C, Behrendt H, Gerards P, Kammermeier H

出版信息

Eur J Cell Biol. 1982 Jun;27(2):262-9.

PMID:6288380
Abstract

A new perfusion medium for isolating cardiac myocytes from adult rats was developed, thereby yielding numerous viable cells with few morphological changes. The main factors in the isolation procedure are Ca2+ deficiency, collagenase, and mechanical dispersion. Their effects on the ultrastructure of cardiac myocytes were separately tested. In isolated hearts, perfusion with a medium containing a physiological Ca2+ concentration (2.5 mM, controls) preserved the cellular fine structure well, whereas perfusion with a medium containing 2.5 mM Ca2+ plus 0.05% collagenase caused swelling and disruption of most cells. Perfusion with a Ca2+-deficient medium followed by a medium with a low Ca2+ concentration (25 microM) either containing or lacking collagenase resulted in widening of the T-tubules, reduced electron density of the external lamina and occasional separation, or even dissolution of this layer. Some cells were damaged and hypercontracted. These appeared more numerous in suspensions, that means after mechanical dispersion of the myocardium. However, most of the isolated cells were regularly shaped (up to 30-60 min as shown in another study) and their ultrastructure was only slightly altered. This corresponds to an adequate preservation of the cell membranes proven in earlier membrane transfer studies.

摘要

开发了一种用于从成年大鼠分离心肌细胞的新型灌注培养基,从而获得了大量形态变化极少的活细胞。分离过程中的主要因素是钙缺乏、胶原酶和机械分散。分别测试了它们对心肌细胞超微结构的影响。在离体心脏中,用含有生理钙浓度(2.5 mM,对照组)的培养基灌注能很好地保存细胞精细结构,而用含有2.5 mM钙加0.05%胶原酶的培养基灌注会导致大多数细胞肿胀和破裂。先用缺钙培养基灌注,然后用含有或不含胶原酶的低钙浓度(25 microM)培养基灌注,会导致T小管增宽、外层电子密度降低以及偶尔的分离,甚至该层的溶解。一些细胞受损并过度收缩。这些在悬浮液中更常见,即在心肌机械分散后。然而,大多数分离的细胞形状规则(如另一项研究所显示,长达30 - 60分钟),其超微结构仅略有改变。这与早期膜转运研究中证明的细胞膜的充分保存相对应。

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