Van Swearingen J, Lance-Jones C
Department of Neurobiology, University of Pittsburgh School of Medicine, Pennyslvania 15261, USA.
Dev Biol. 1995 Aug;170(2):321-37. doi: 10.1006/dbio.1995.1218.
Avian limb myoblasts originate from somites and migrate into the periphery during limb bud formation. It is not known how these precursors become arranged into a stereotyped pattern of muscles and primary fiber types. We used in vivo surgical transplantation and anatomical analyses of thigh muscle patterns to ask whether myoblasts migrating into the limb bud at different developmental times adopt different fates. When myoblast migration was interrupted by transplanting limb bud tissue to the coelomic cavity of a host embryo early in the migratory period (stages 16-early 17), few thigh muscles were found at stages 30-33. Primordia that were present corresponded to muscles that normally contain a majority of slow myotubes. In limbs transplanted slightly later (stages late 17-18), the only missing muscles were those that normally contain the highest numbers of fast myotubes. Parallel results were obtained in chimeric limbs made by transplanting a quail limb bud to a chick host at different times during the migratory period, an experimental situation in which the limbs were not depleted of muscle precursors or nerves. These findings suggest that the earliest myoblast migrants give rise mainly to slow primary myotubes, the later migrants to fast myotubes. To determine whether the early limb bud environment defines the fate of migrating myoblasts, we assessed fiber type patterns in limbs that developed from young limb bud tissue (stages 15-early 16) transplanted to older hosts (stage 17). A significant depletion of slow myosin-positive profiles was found within slow muscles. Fast muscles were generally normal in size. These results provide in vivo evidence that limb myoblast diversity arises prior to the entry of myoblasts into the limb. We suggest that there is a gradual change in the proportions of myoblasts capable of forming slow and fast fiber types, a change which may begin in the somites or early in the migratory period.
禽类肢体成肌细胞起源于体节,并在肢体芽形成过程中迁移至外周。目前尚不清楚这些前体细胞是如何排列成肌肉和初级纤维类型的定型模式的。我们通过体内手术移植和大腿肌肉模式的解剖分析来探究在不同发育时期迁移到肢体芽中的成肌细胞是否会有不同的命运。当在迁移期早期(第16阶段 - 第17阶段早期)将肢体芽组织移植到宿主胚胎的体腔中从而中断成肌细胞迁移时,在第30 - 33阶段几乎未发现大腿肌肉。存在的原基对应于通常含有大多数慢肌管的肌肉。在稍晚些时候(第17阶段晚期 - 第18阶段)移植的肢体中,唯一缺失的肌肉是那些通常含有最多快肌管的肌肉。在迁移期的不同时间将鹌鹑肢体芽移植到鸡宿主中制成的嵌合肢体中也获得了类似结果,在这种实验情况下,肢体并未耗尽肌肉前体细胞或神经。这些发现表明,最早迁移的成肌细胞主要产生慢初级肌管,较晚迁移的成肌细胞产生快肌管。为了确定早期肢体芽环境是否决定迁移中成肌细胞的命运,我们评估了由移植到较老宿主(第17阶段)的年轻肢体芽组织(第15阶段 - 第16阶段早期)发育而来的肢体中的纤维类型模式。在慢肌中发现慢肌球蛋白阳性轮廓显著减少。快肌的大小通常正常。这些结果提供了体内证据,表明肢体成肌细胞的多样性在成肌细胞进入肢体之前就已出现。我们认为,能够形成慢纤维和快纤维类型的成肌细胞比例存在逐渐变化,这种变化可能始于体节或迁移期早期。