Yutzey K, Gannon M, Bader D
Department of Cell Biology and Anatomy, Cornell University Medical College, New York, New York 10021, USA.
Dev Biol. 1995 Aug;170(2):531-41. doi: 10.1006/dbio.1995.1234.
The ability of undifferentiated cardiogenic mesoderm to generate diversified myogenic phenotypes was assayed in a minimal culture system. During cardiogenesis in vivo, the anterior and posterior segments of the avian heart have distinct patterns of contractile protein gene expression when they first differentiate. To assess the potential of undifferentiated cardiogenic tissue to diversify into distinct anterior and posterior lineages prior to heart formation, cardiogenic mesoderm and endoderm were removed together from the embryo at Hamburger and Hamilton stages 4-8. Explants from each of these stages differentiated in defined medium as indicated by the expression of muscle-specific genes. However, the ability to express the atrial-specific myosin heavy chain (AMHC) mRNA was confined to posterior cardiac progenitors. Diversification was not dependent on anterior endoderm, suggesting that inductive interactions between the mesoderm and endoderm are not necessary to maintain diversified cardiac lineages after stage 4. The diversified potential of explanted cardiogenic tissue was altered with retinoic acid treatment, resulting in the activation of AMHC1 gene expression in the anterior progenitors. Anterior cardiogenic cells removed from the embryo at stage 8, when the heart begins to differentiate in vivo, are not susceptible to the alteration of diversified phenotype by retinoic acid treatment. Therefore, the potential to form distinct cardiomyogenic cell lineages is present in the anterior lateral plate mesoderm soon after gastrulation and the maturation of these lineages in a positionally dependent manner is maintained in a simple defined culture system in vitro.
在一个简易培养系统中检测了未分化的心脏中胚层产生多样化肌源性表型的能力。在体内心脏发生过程中,鸡胚心脏的前段和后段在首次分化时具有不同的收缩蛋白基因表达模式。为了评估未分化的心脏组织在心脏形成之前分化为不同的前侧和后侧谱系的潜力,在汉伯格和汉密尔顿4 - 8期从胚胎中一起移除心脏中胚层和内胚层。这些阶段的外植体在特定培养基中分化,这通过肌肉特异性基因的表达得以体现。然而,表达心房特异性肌球蛋白重链(AMHC)mRNA的能力仅限于后侧心脏祖细胞。分化并不依赖于前侧内胚层,这表明中胚层和内胚层之间的诱导相互作用对于维持4期之后的多样化心脏谱系并非必要。用视黄酸处理可改变移植的心脏组织的多样化潜力,导致前侧祖细胞中AMHC1基因表达的激活。在体内心脏开始分化的8期从胚胎中移除的前侧心脏细胞,对视黄酸处理引起的多样化表型改变不敏感。因此,在原肠胚形成后不久,前侧侧板中胚层就具有形成不同心肌细胞谱系的潜力,并且这些谱系在体外简单的特定培养系统中以位置依赖的方式维持其成熟状态。