21-P042 Receptor protein tyrosine phosphatases as potential regulators of neurotrophin receptors in developing sensory neurons
نویسندگان
چکیده
Vertebrates have two pairs of morphologically distinct appendages, the forelimbs and the hindlimbs. Although the mechanisms necessary for limb outgrowth and polarity are becoming fairly well-understood little is known about how limb-type identity is regulated. The homeobox containing transcription factor Pitx1 expressed in hindlimb bud mesenchyme and has been shown to be involved in limb-type determination. A complication to the interpretation of the Pitx1 phenotype has arisen following the demonstration that Pitx1 activity is required for normal expression of Tbx4. Since Tbx4 is required for normal limb outgrowth some of the abnormalities observed in the Pitx1 hindlimb could be explained by down regulation of Tbx4. We are using transgenic lines expressing Tbx4, Tbx5 or Pitx1 in combination with Pitx1 mouse to study the activity of Pitx1 independently of outgrowth defects. Both Tbx4 and Tbx5 rescued hindlimbs are closer to a wild-type size but none of the hindlimb characteristics are compensated by the expression of these T-box genes. Our data show that Pitx1 function is necessary for hindlimb patterning and is consistent with Tbx4 and Tbx5 being insufficient to determine limb-type but contributing to limb initiation and outgrowth.
منابع مشابه
Developmental co-expression and functional redundancy of tyrosine phosphatases with neurotrophin receptors in developing sensory neurons.
Receptor-type protein tyrosine phosphatases (RPTPs) have been implicated as direct or indirect regulators of neurotrophin receptors (TRKs). It remains less clear if and how such RPTPs might regulate TRK proteins in vivo during development. Here we present a comparative expression profile of RPTP genes and Trk genes during early stages of murine, dorsal root ganglion maturation. We find little i...
متن کاملExpression and binding characteristics of the BDNF receptor chick trkB.
Previous studies using transfected cells have indicated that the mammalian receptor tyrosine kinase trkB binds the neurotrophins brain-derived neurotrophic factor, neurotrophin-3 and neurotrophin-4. However, most studies demonstrating that these neurotrophins prevent the death of embryonic neurons and have specific neuronal receptors have been performed with chick neurons. In order to explore t...
متن کاملCharacterization of Neurotrophin and Trk Receptor Functions in Developing Sensory Ganglia Direct NT-3 Activation of TrkB Neurons In Vivo
Spinal sensory ganglia have been shown to contain neuronal subpopulations with different functions and neurotrophin dependencies. Neurotrophins act, in large part, through Trk receptor tyrosine kinases: nerve growth factor (NGF) via TrkA, brain-derived neurotrophic factor (BDNF) and neurotrophin-4/5 (NT-4/5) via TrkB, and neurotrophin-3 (NT-3) via TrkC. In the present paper, we use antibodies t...
متن کاملShcB and ShcC activation by the Trk family of receptor tyrosine kinases.
Activation of the neurotrophin Trk receptors is a key process in the survival and development of the nervous system. The signaling adapters ShcB and ShcC, but not ShcA, are thought to be the primary Shc adaptor proteins in neurons as both are highly expressed in both the developing and adult nervous system. Although a previous study suggested that ShcB and ShcC do not strongly interact with the...
متن کاملCell Survival through Trk Neurotrophin Receptors Is Differentially Regulated by Ubiquitination
Specificity of neurotrophin factor signaling is dictated through the action of Trk receptor tyrosine kinases. Once activated, Trk receptors are internalized and targeted for degradation. However, the mechanisms implicated in this process are incompletely understood. Here we report that the Trk receptors are multimonoubiquitinated in response to neurotrophins. We have identified an E3 ubiquitin ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Mechanisms of Development
دوره 126 شماره
صفحات -
تاریخ انتشار 2009