首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Cellular invasion of the chicken corneal stroma during development: Regulation by multiple matrix metalloproteases and the lens.
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Cellular invasion of the chicken corneal stroma during development: Regulation by multiple matrix metalloproteases and the lens.

机译:发育过程中鸡角膜基质的细胞浸润:由多种基质金属蛋白酶和晶状体调控。

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Avian corneal development requires cellular invasion into the acellular matrix of the primary stroma. Previous results show that this invasion is preceded by the removal of the fibril-associated type IX collagen, which possibly stabilizes matrices through interfibrillar cross-bridges secured by covalent crosslinks. In the present study, we provide evidence for the expression of three matrix metalloproteinases (MMPs) in early corneas, two of which act cooperatively to selectively remove type IX collagen in situ. In organ cultures, MMP inhibitors (either TIMP-2 or a synthetic inhibitor) resulted in arrested development, in which collagen IX persisted, and the stroma remained compact and acellular. We also show that blocking covalent crosslinking of collagen allows for cellular invasion to occur, even when the removal of type IX collagen is prevented. Thus, one factor regulating corneal invasion is the physical structure of the matrix, which can be modified by either selective proteolysis or reducing interfibrillar cross-bridges. We also detected another level of regulation of cellular invasion involving inhibition by the underlying lens. This block, which seems to influence invasive behavior independently of matrix modification, is a transient event that is released in ovo just before invasion proceeds. Developmental Dynamics 232:106-118, 2005. (c) 2004 Wiley-Liss, Inc.
机译:禽角膜发育需要细胞侵入原代基质的无细胞基质。先前的结果表明,这种侵袭是在去除原纤维相关的IX型胶原蛋白之前进行的,该蛋白可能通过通过共价交联键固定的原纤维间跨桥来稳定基质。在本研究中,我们为早期角膜中三种基质金属蛋白酶(MMP)的表达提供了证据,其中两种协同作用以选择性地原位去除IX型胶原。在器官培养物中,MMP抑制剂(TIMP-2或合成抑制剂)导致停滞发展,其中胶原蛋白IX持续存在,并且基质保持致密和无细胞。我们还表明,阻断胶原蛋白的共价交联即使发生IX型胶原蛋白去除的情况下,也允许细胞入侵。因此,调节角膜浸润的一个因素是基质的物理结构,其可以通过选择性蛋白水解或减少原纤维间的跨桥而改变。我们还检测到细胞入侵的另一种调控水平,涉及到潜在晶状体的抑制。这个障碍似乎独立于基质修饰而影响侵入行为,是一个瞬时事件,在侵入进行之前就在卵中释放。发展动力学232:106-118,2005.(c)2004 Wiley-Liss,Inc.

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